Linked Data
ClinVar Variation Id:
1155
ClinVar RCV Id:
RCV000001214
dbSNP Id:
rs121918194
ExAC:
12:48535824 A / C
gnomAD v2:
12-48535824-A-C
gnomAD v4:
12-48142041-A-C
PubMed:
PMID:7513946
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48142041A>C , CM000674.2:g.48142041A>C | GRCh38 |
| NC_000012.11:g.48535824A>C , CM000674.1:g.48535824A>C | GRCh37 |
| NC_000012.10:g.46822091A>C | NCBI36 |
| NG_016199.1:g.41169A>C | |
| NG_016199.2:g.41789A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000550257.7:c.1850A>C | ENSP00000447997.3:p.Asp617Ala | |
| ENST00000340802.12:c.1841A>C | ENSP00000345771.6:p.Asp614Ala | |
| ENST00000359794.11:c.1628A>C MANE Select | ENSP00000352842.5:p.Asp543Ala | |
| ENST00000549941.7:c.1535A>C | ENSP00000446829.3:p.Asp512Ala | |
| ENST00000550345.6:c.1628A>C | ENSP00000450369.2:p.Asp543Ala | |
| ENST00000550924.6:c.1628A>C | ENSP00000446945.2:p.Asp543Ala | |
| ENST00000551339.6:c.1628A>C | ENSP00000448253.2:p.Asp543Ala | |
| ENST00000642730.1:c.1937A>C | ENSP00000496597.1:p.Asp646Ala | |
| ENST00000312352.11:c.1628A>C | ENSP00000309438.7:p.Asp543Ala | |
| ENST00000340802.10:c.1841A>C | ENSP00000345771.6:p.Asp614Ala | |
| ENST00000359794.9:c.1628A>C | ENSP00000352842.5:p.Asp543Ala | |
| ENST00000546465.1:c.473A>C | ENSP00000446519.1:p.Asp158Ala | |
| ENST00000546964.5:n.1952A>C | ||
| ENST00000547581.5:c.*1896A>C | ENSP00000447992.1:n.*1896A>C | |
| ENST00000547587.5:c.1628A>C | ENSP00000449426.1:p.Asp543Ala | |
| ENST00000550802.1:n.346A>C | ||
| ENST00000551804.5:c.1535A>C | ENSP00000448177.1:p.Asp512Ala | |
| ENST00000552214.1:n.284A>C | ||
| ENST00000552752.5:c.777A>C | ||
| ENST00000552818.1:n.251A>C | ||
| ENST00000553055.1:c.69A>C | ||
| NM_000289.5:c.1628A>C | NP_000280.1:p.Asp543Ala | |
| NM_001166686.1:c.1841A>C | NP_001160158.1:p.Asp614Ala | |
| NM_001166687.1:c.1628A>C | NP_001160159.1:p.Asp543Ala | |
| NM_001166688.1:c.1628A>C | NP_001160160.1:p.Asp543Ala | |
| XM_005268974.1:c.1937A>C | XP_005269031.1:p.Asp646Ala | |
| XM_005268975.1:c.1937A>C | XP_005269032.1:p.Asp646Ala | |
| XM_005268976.2:c.1937A>C | XP_005269033.1:p.Asp646Ala | |
| XM_005268977.1:c.1841A>C | XP_005269034.1:p.Asp614Ala | |
| XM_005268978.2:c.1841A>C | XP_005269035.1:p.Asp614Ala | |
| XM_005268979.1:c.1841A>C | XP_005269036.1:p.Asp614Ala | |
| XM_011538487.1:c.1844A>C | XP_011536789.1:p.Asp615Ala | |
| XM_011538488.1:c.1628A>C | XP_011536790.1:p.Asp543Ala | |
| NM_000289.6:c.1628A>C MANE Select | NP_000280.1:p.Asp543Ala | |
| NM_001166686.2:c.1841A>C | NP_001160158.1:p.Asp614Ala | |
| NM_001354735.1:c.1937A>C | NP_001341664.1:p.Asp646Ala | |
| NM_001354736.1:c.1937A>C | NP_001341665.1:p.Asp646Ala | |
| NM_001354737.1:c.1841A>C | NP_001341666.1:p.Asp614Ala | |
| NM_001354738.1:c.1841A>C | NP_001341667.1:p.Asp614Ala | |
| NM_001354739.1:c.1841A>C | NP_001341668.1:p.Asp614Ala | |
| NM_001354740.1:c.1772A>C | NP_001341669.1:p.Asp591Ala | |
| NM_001354741.1:c.1652A>C | NP_001341670.1:p.Asp551Ala | |
| NM_001354742.1:c.1628A>C | NP_001341671.1:p.Asp543Ala | |
| NM_001354743.1:c.1628A>C | NP_001341672.1:p.Asp543Ala | |
| NM_001354744.1:c.1628A>C | NP_001341673.1:p.Asp543Ala | |
| NM_001354745.1:c.1541A>C | NP_001341674.1:p.Asp514Ala | |
| NM_001354746.1:c.1502A>C | NP_001341675.1:p.Asp501Ala | |
| NM_001354747.1:c.1478A>C | NP_001341676.1:p.Asp493Ala | |
| NM_001354748.1:c.1478A>C | NP_001341677.1:p.Asp493Ala | |
| NM_001363619.1:c.1535A>C | NP_001350548.1:p.Asp512Ala | |
| NR_148954.1:n.2065A>C | ||
| NR_148955.1:n.2701A>C | ||
| NR_148956.1:n.1991A>C | ||
| NR_148957.1:n.2220A>C | ||
| NR_148958.1:n.1968A>C | ||
| NR_148959.1:n.1894A>C | ||
| XM_005268976.3:c.1937A>C | XP_005269033.1:p.Asp646Ala | |
| XM_017019469.1:c.1748A>C | XP_016874958.1:p.Asp583Ala | |
| XM_024449020.1:c.1850A>C | XP_024304788.1:p.Asp617Ala | |
| XM_024449021.1:c.1727A>C | XP_024304789.1:p.Asp576Ala | |
| XM_024449022.1:c.1628A>C | XP_024304790.1:p.Asp543Ala | |
| NM_001166687.2:c.1628A>C | NP_001160159.1:p.Asp543Ala | |
| NM_001166688.2:c.1628A>C | NP_001160160.1:p.Asp543Ala | |
| NM_001354741.2:c.1652A>C | NP_001341670.1:p.Asp551Ala | |
| NM_001354742.2:c.1628A>C | NP_001341671.1:p.Asp543Ala | |
| NM_001354743.2:c.1628A>C | NP_001341672.1:p.Asp543Ala | |
| NM_001354744.2:c.1628A>C | NP_001341673.1:p.Asp543Ala | |
| NM_001354745.2:c.1541A>C | NP_001341674.1:p.Asp514Ala | |
| NM_001354746.2:c.1502A>C | NP_001341675.1:p.Asp501Ala | |
| NM_001354747.2:c.1478A>C | NP_001341676.1:p.Asp493Ala | |
| NM_001354748.2:c.1478A>C | NP_001341677.1:p.Asp493Ala | |
| NM_001363619.2:c.1535A>C | NP_001350548.1:p.Asp512Ala | |
| NR_148954.2:n.1931A>C | ||
| NR_148956.2:n.1857A>C | ||
| NR_148957.2:n.2086A>C | ||
| NR_148958.2:n.1834A>C | ||
| NR_148959.2:n.1760A>C |