UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
MyVariant Identifiers:
chr2:g.70439935T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.70212803T>A , CM000664.2:g.70212803T>A | GRCh38 |
| NC_000002.11:g.70439935T>A , CM000664.1:g.70439935T>A | GRCh37 |
| NC_000002.10:g.70293439T>A | NCBI36 |
| NG_029967.1:g.40845A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000433529.7:c.1077A>T (TIA1) MANE Select | ENSP00000401371.2:p.Gly359= | |
| ENST00000282574.8:c.1074A>T (TIA1) | ENSP00000282574.4:p.Gly358= | |
| ENST00000415783.6:c.1044A>T (TIA1) | ENSP00000404023.2:p.Gly348= | |
| ENST00000433529.6:c.1077A>T (TIA1) | ENSP00000401371.2:p.Gly359= | |
| ENST00000445587.5:c.774A>T (TIA1) | ENSP00000399567.1:p.Gly258= | |
| ENST00000470096.1:n.212-30806A>T (C2orf42) | ||
| ENST00000486392.5:n.387A>T (TIA1) | ||
| ENST00000495774.1:n.479A>T (TIA1) | ||
| NM_022037.2:c.1044A>T (TIA1) | NP_071320.2:p.Gly348= | |
| NM_022173.2:c.1077A>T (TIA1) | NP_071505.2:p.Gly359= | |
| XM_005264527.1:c.1041A>T (TIA1) | XP_005264584.1:p.Gly347= | |
| XM_005264528.3:c.882A>T (TIA1) | XP_005264585.1:p.Gly294= | |
| XM_005264531.1:c.774A>T (TIA1) | XP_005264588.1:p.Gly258= | |
| XM_011533077.1:c.1074A>T (TIA1) | XP_011531379.1:p.Gly358= | |
| XM_011533078.1:c.777A>T (TIA1) | XP_011531380.1:p.Gly259= | |
| XM_011533079.1:c.777A>T (TIA1) | XP_011531381.1:p.Gly259= | |
| XM_011533080.1:c.777A>T (TIA1) | XP_011531382.1:p.Gly259= | |
| XM_011533081.1:c.777A>T (TIA1) | XP_011531383.1:p.Gly259= | |
| XM_011533082.1:c.777A>T (TIA1) | XP_011531384.1:p.Gly259= | |
| XM_011533083.1:c.657A>T (TIA1) | XP_011531385.1:p.Gly219= | |
| XR_244955.1:n.1434A>T (TIA1) | ||
| XR_939714.1:n.1413A>T (TIA1) | ||
| NM_001351508.1:c.1074A>T (TIA1) | NP_001338437.1:p.Gly358= | |
| NM_001351509.1:c.1050A>T (TIA1) | NP_001338438.1:p.Gly350= | |
| NM_001351510.1:c.1041A>T (TIA1) | NP_001338439.1:p.Gly347= | |
| NM_001351511.1:c.966A>T (TIA1) | NP_001338440.1:p.Gly322= | |
| NM_001351512.1:c.939A>T (TIA1) | NP_001338441.1:p.Gly313= | |
| NM_001351513.1:c.933A>T (TIA1) | NP_001338442.1:p.Gly311= | |
| NM_001351514.1:c.849A>T (TIA1) | NP_001338443.1:p.Gly283= | |
| NM_001351515.1:c.774A>T (TIA1) | NP_001338444.1:p.Gly258= | |
| NM_001351517.1:c.654A>T (TIA1) | NP_001338446.1:p.Gly218= | |
| NM_001351524.1:c.657A>T (TIA1) | NP_001338453.1:p.Gly219= | |
| NM_001351525.1:c.657A>T (TIA1) | NP_001338454.1:p.Gly219= | |
| NM_022037.3:c.1044A>T (TIA1) | NP_071320.2:p.Gly348= | |
| NM_022173.3:c.1077A>T (TIA1) | NP_071505.2:p.Gly359= | |
| NR_147216.1:n.1434A>T (TIA1) | ||
| NR_147217.1:n.1315A>T (TIA1) | ||
| NR_147218.1:n.1312A>T (TIA1) | ||
| NR_147219.1:n.1549A>T (TIA1) | ||
| NR_147220.1:n.1535A>T (TIA1) | ||
| NR_147221.1:n.1606A>T (TIA1) | ||
| NR_147222.1:n.1601A>T (TIA1) | ||
| NR_147223.1:n.1659A>T (TIA1) | ||
| NR_147224.1:n.1537A>T (TIA1) | ||
| NR_147225.1:n.1692A>T (TIA1) | ||
| NR_147226.1:n.1540A>T (TIA1) | ||
| NR_147227.1:n.1610A>T (TIA1) | ||
| NR_147228.1:n.1573A>T (TIA1) | ||
| NR_147229.1:n.1516A>T (TIA1) | ||
| NR_147230.1:n.1758A>T (TIA1) | ||
| NR_147231.1:n.1570A>T (TIA1) | ||
| NR_147232.1:n.1443A>T (TIA1) | ||
| XM_005264528.5:c.882A>T (TIA1) | XP_005264585.1:p.Gly294= | |
| XM_005264531.2:c.774A>T (TIA1) | XP_005264588.1:p.Gly258= | |
| XM_011533082.2:c.777A>T (TIA1) | XP_011531384.1:p.Gly259= | |
| XM_017004792.1:c.777A>T (TIA1) | XP_016860281.1:p.Gly259= | |
| XM_017004793.2:c.777A>T (TIA1) | XP_016860282.1:p.Gly259= | |
| XM_017004794.1:c.777A>T (TIA1) | XP_016860283.1:p.Gly259= | |
| XM_017004795.1:c.774A>T (TIA1) | XP_016860284.1:p.Gly258= | |
| XM_017004796.1:c.657A>T (TIA1) | XP_016860285.1:p.Gly219= | |
| XM_017004800.1:c.657A>T (TIA1) | XP_016860289.1:p.Gly219= | |
| XM_024453063.1:c.657A>T (TIA1) | XP_024308831.1:p.Gly219= | |
| XM_024453064.1:c.657A>T (TIA1) | XP_024308832.1:p.Gly219= | |
| XM_024453065.1:c.657A>T (TIA1) | XP_024308833.1:p.Gly219= | |
| XM_024453066.1:c.657A>T (TIA1) | XP_024308834.1:p.Gly219= | |
| XM_024453067.1:c.654A>T (TIA1) | XP_024308835.1:p.Gly218= | |
| XR_002959329.1:n.4661A>T (TIA1) | ||
| XR_002959330.1:n.2495A>T (TIA1) | ||
| XR_002959331.1:n.4658A>T (TIA1) | ||
| XR_002959332.1:n.2201A>T (TIA1) | ||
| NM_022173.4:c.1077A>T (TIA1) MANE Select | NP_071505.2:p.Gly359= | |
| NM_001351508.2:c.1074A>T (TIA1) | NP_001338437.1:p.Gly358= | |
| NM_001351509.2:c.1050A>T (TIA1) | NP_001338438.1:p.Gly350= | |
| NM_001351510.2:c.1041A>T (TIA1) | NP_001338439.1:p.Gly347= | |
| NM_001351514.2:c.849A>T (TIA1) | NP_001338443.1:p.Gly283= | |
| NM_001351515.2:c.774A>T (TIA1) | NP_001338444.1:p.Gly258= | |
| NM_001351517.2:c.654A>T (TIA1) | NP_001338446.1:p.Gly218= | |
| NM_001351524.2:c.657A>T (TIA1) | NP_001338453.1:p.Gly219= | |
| NM_001351525.2:c.657A>T (TIA1) | NP_001338454.1:p.Gly219= | |
| NM_022037.4:c.1044A>T (TIA1) | NP_071320.2:p.Gly348= | |
| NR_147219.2:n.1384A>T (TIA1) | ||
| NR_147220.2:n.1370A>T (TIA1) | ||
| NR_147221.2:n.1441A>T (TIA1) | ||
| NR_147222.2:n.1436A>T (TIA1) | ||
| NR_147223.2:n.1494A>T (TIA1) | ||
| NR_147224.2:n.1372A>T (TIA1) | ||
| NR_147225.2:n.1527A>T (TIA1) | ||
| NR_147226.2:n.1375A>T (TIA1) | ||
| NR_147227.2:n.1445A>T (TIA1) | ||
| NR_147228.2:n.1408A>T (TIA1) | ||
| NR_147229.2:n.1351A>T (TIA1) | ||
| NR_147230.2:n.1593A>T (TIA1) | ||
| NR_147231.2:n.1405A>T (TIA1) | ||
| NR_147232.2:n.1278A>T (TIA1) |