Linked Data
ClinVar Variation Id:
94679
ClinVar RCV Id:
RCV000080669
RCV000405962
RCV000617606
RCV000711462
RCV001083252
RCV001831861
RCV002504993
dbSNP Id:
rs143159113
ExAC:
X:32361266 A / G
gnomAD v2:
X-32361266-A-G
gnomAD v3:
X-32343149-A-G
gnomAD v4:
X-32343149-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.32343149A>G , CM000685.2:g.32343149A>G | GRCh38 |
| NC_000023.10:g.32361266A>G , CM000685.1:g.32361266A>G | GRCh37 |
| NC_000023.9:g.32271187A>G | NCBI36 |
| NG_012232.1:g.1001461T>C , LRG_199:g.1001461T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.570T>C | ENSP00000350765.3:p.Asp190= | |
| ENST00000357033.9:c.5724T>C MANE Select | ENSP00000354923.3:p.Asp1908= | |
| ENST00000619831.5:c.1692T>C | ENSP00000479270.2:p.Asp564= | |
| ENST00000357033.8:c.5724T>C | ENSP00000354923.3:p.Asp1908= | |
| ENST00000378677.6:c.5712T>C | ENSP00000367948.2:p.Asp1904= | |
| ENST00000488902.5:n.336-126086T>C | ||
| ENST00000493412.1:c.381T>C | ENSP00000417725.1:p.Asp127= | |
| ENST00000619831.4:c.5712T>C | ENSP00000479270.1:p.Asp1904= | |
| ENST00000620040.4:c.5724T>C | ENSP00000478150.1:p.Asp1908= | |
| NM_000109.3:c.5700T>C | NP_000100.2:p.Asp1900= | |
| NM_004006.2:c.5724T>C , LRG_199t1:c.5724T>C | NP_003997.1:p.Asp1908= | |
| NM_004009.3:c.5712T>C | NP_004000.1:p.Asp1904= | |
| NM_004010.3:c.5355T>C | NP_004001.1:p.Asp1785= | |
| NM_004011.3:c.1701T>C | NP_004002.2:p.Asp567= | |
| NM_004012.3:c.1692T>C | NP_004003.1:p.Asp564= | |
| XM_006724468.2:c.5724T>C | XP_006724531.1:p.Asp1908= | |
| XM_006724469.2:c.5700T>C | XP_006724532.1:p.Asp1900= | |
| XM_006724470.2:c.5724T>C | XP_006724533.1:p.Asp1908= | |
| XM_006724471.2:c.5724T>C | XP_006724534.1:p.Asp1908= | |
| XM_006724472.2:c.5595T>C | XP_006724535.1:p.Asp1865= | |
| XM_006724473.2:c.5586T>C | XP_006724536.1:p.Asp1862= | |
| XM_006724474.2:c.5724T>C | XP_006724537.1:p.Asp1908= | |
| XM_006724475.2:c.5724T>C | XP_006724538.1:p.Asp1908= | |
| XM_011545467.1:c.5601T>C | XP_011543769.1:p.Asp1867= | |
| XM_011545468.1:c.5724T>C | XP_011543770.1:p.Asp1908= | |
| XM_011545469.1:c.5724T>C | XP_011543771.1:p.Asp1908= | |
| XM_006724469.3:c.5700T>C | XP_006724532.1:p.Asp1900= | |
| XM_006724470.3:c.5724T>C | XP_006724533.1:p.Asp1908= | |
| XM_006724474.3:c.5724T>C | XP_006724537.1:p.Asp1908= | |
| XM_011545468.2:c.5724T>C | XP_011543770.1:p.Asp1908= | |
| XM_017029328.1:c.5724T>C | XP_016884817.1:p.Asp1908= | |
| XM_017029329.1:c.5724T>C | XP_016884818.1:p.Asp1908= | |
| XM_017029330.2:c.5724T>C | XP_016884819.1:p.Asp1908= | |
| NM_000109.4:c.5700T>C | NP_000100.3:p.Asp1900= | |
| NM_004006.3:c.5724T>C MANE Select | NP_003997.2:p.Asp1908= | |
| NM_004011.4:c.1701T>C | NP_004002.3:p.Asp567= | |
| NM_004012.4:c.1692T>C | NP_004003.2:p.Asp564= |