Linked Data
dbSNP Id:
rs1483639651
gnomAD v3:
4-102598419-A-AGAAATCCTTT
gnomAD v4:
4-102598419-A-AGAAATCCTTT
MyVariant Identifiers:
chr4:g.103519576_103519577insGAAATCCTTT (hg19)
chr4:g.102598419_102598420insGAAATCCTTT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.102598420_102598429dup , CM000666.2:g.102598420_102598429dup | GRCh38 |
| NC_000004.11:g.103519577_103519586dup , CM000666.1:g.103519577_103519586dup | GRCh37 |
| NC_000004.10:g.103738615_103738624dup | NCBI36 |
| NG_050628.1:g.102092_102101dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000507079.6:c.1661+759_1661+768dup | ENSP00000426147.2:n.1661+759_1661+768dup | |
| ENST00000509165.2:c.1637+759_1637+768dup | ENSP00000423877.2:n.1637+759_1637+768dup | |
| ENST00000697794.1:c.*1278+759_*1278+768dup | ENSP00000513443.1:n.*1278+759_*1278+768dup | |
| ENST00000697799.1:n.1134+759_1134+768dup | ||
| ENST00000698233.1:n.1366+759_1366+768dup | ||
| ENST00000226574.9:c.1637+759_1637+768dup MANE Select | ENSP00000226574.4:n.1637+759_1637+768dup | |
| ENST00000652569.1:c.1613+759_1613+768dup | ||
| ENST00000652619.1:c.*164+759_*164+768dup | ENSP00000499031.1:n.*164+759_*164+768dup | |
| ENST00000226574.8:c.1637+759_1637+768dup | ENSP00000226574.4:n.1637+759_1637+768dup | |
| ENST00000394820.8:c.1634+759_1634+768dup | ENSP00000378297.4:n.1634+759_1634+768dup | |
| ENST00000505458.5:c.1634+759_1634+768dup | ENSP00000424790.1:n.1634+759_1634+768dup | |
| ENST00000600343.5:c.1094+759_1094+768dup | ENSP00000469340.1:n.1094+759_1094+768dup | |
| NM_001165412.1:c.1634+759_1634+768dup | NP_001158884.1:n.1634+759_1634+768dup | |
| NM_003998.3:c.1637+759_1637+768dup | NP_003989.2:n.1637+759_1637+768dup | |
| XM_011532006.1:c.1658+759_1658+768dup | XP_011530308.1:n.1658+759_1658+768dup | |
| XM_011532007.1:c.1634+759_1634+768dup | XP_011530309.1:n.1634+759_1634+768dup | |
| XM_011532008.1:c.1478+759_1478+768dup | XP_011530310.1:n.1478+759_1478+768dup | |
| XM_011532009.1:c.1241+759_1241+768dup | XP_011530311.1:n.1241+759_1241+768dup | |
| XR_939027.1:n.3898_3907dup | ||
| NM_001319226.1:c.1634+759_1634+768dup | NP_001306155.1:n.1634+759_1634+768dup | |
| XM_011532006.2:c.1658+759_1658+768dup | XP_011530308.1:n.1658+759_1658+768dup | |
| XM_024454067.1:c.1661+759_1661+768dup | XP_024309835.1:n.1661+759_1661+768dup | |
| XM_024454068.1:c.1637+759_1637+768dup | XP_024309836.1:n.1637+759_1637+768dup | |
| XM_024454069.1:c.1502+759_1502+768dup | XP_024309837.1:n.1502+759_1502+768dup | |
| NM_003998.4:c.1637+759_1637+768dup MANE Select | NP_003989.2:n.1637+759_1637+768dup | |
| NM_001165412.2:c.1634+759_1634+768dup | NP_001158884.1:n.1634+759_1634+768dup | |
| NM_001319226.2:c.1634+759_1634+768dup | NP_001306155.1:n.1634+759_1634+768dup | |
| NM_001382625.1:c.1637+759_1637+768dup | NP_001369554.1:n.1637+759_1637+768dup | |
| NM_001382626.1:c.1637+759_1637+768dup | NP_001369555.1:n.1637+759_1637+768dup | |
| NM_001382627.1:c.1634+759_1634+768dup | NP_001369556.1:n.1634+759_1634+768dup | |
| NM_001382628.1:c.1595+759_1595+768dup | NP_001369557.1:n.1595+759_1595+768dup |