Linked Data
ClinVar Variation Id:
557399
ClinVar RCV Id:
RCV000673535
dbSNP Id:
rs1555528803
gnomAD v2:
17-7127384-G-A
gnomAD v4:
17-7224065-G-A
MyVariant Identifiers:
chr17:g.7127384G>A (hg19)
chr17:g.7127384_7127386delinsATA (hg19)
chr17:g.7224065G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7224065G>A , CM000679.2:g.7224065G>A | GRCh38 |
| NC_000017.10:g.7127384G>A , CM000679.1:g.7127384G>A | GRCh37 |
| NC_000017.9:g.7068108G>A | NCBI36 |
| NG_007975.1:g.9232G>A | |
| NG_008391.2:g.986C>T | |
| NG_033038.1:g.15480C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.1430G>A MANE Select | ENSP00000349297.5:p.Cys477Tyr | |
| ENST00000322910.9:c.*1385G>A | ENSP00000325395.5:n.*1385G>A | |
| ENST00000350303.9:c.1364G>A | ENSP00000344152.5:p.Cys455Tyr | |
| ENST00000356839.9:c.1430G>A | ENSP00000349297.5:p.Cys477Tyr | |
| ENST00000542255.6:c.288G>A | ||
| ENST00000543245.6:c.1499G>A | ENSP00000438689.2:p.Cys500Tyr | |
| ENST00000578711.1:n.561G>A | ||
| ENST00000579425.5:n.546G>A | ||
| ENST00000579546.1:c.267G>A | ||
| ENST00000579894.5:n.141G>A | ||
| ENST00000583074.5:n.149G>A | ||
| ENST00000583850.5:n.205G>A | ||
| ENST00000583858.5:c.459G>A | ||
| ENST00000585203.6:n.621G>A | ||
| NM_000018.3:c.1430G>A | NP_000009.1:p.Cys477Tyr | |
| NM_001033859.2:c.1364G>A | NP_001029031.1:p.Cys455Tyr | |
| NM_001270447.1:c.1499G>A | NP_001257376.1:p.Cys500Tyr | |
| NM_001270448.1:c.1202G>A | NP_001257377.1:p.Cys401Tyr | |
| XM_006721516.2:c.1430G>A | XP_006721579.2:p.Cys477Tyr | |
| XM_011523829.1:c.1430G>A | XP_011522131.1:p.Cys477Tyr | |
| XM_011523830.1:c.1430G>A | XP_011522132.1:p.Cys477Tyr | |
| XR_934021.1:n.1537G>A | ||
| XR_934022.1:n.1537G>A | ||
| XR_934023.1:n.1537G>A | ||
| XM_006721516.3:c.1430G>A | XP_006721579.2:p.Cys477Tyr | |
| XM_011523829.2:c.1430G>A | XP_011522131.1:p.Cys477Tyr | |
| XM_011523830.2:c.1430G>A | XP_011522132.1:p.Cys477Tyr | |
| XM_024450741.1:c.1430G>A | XP_024306509.1:p.Cys477Tyr | |
| XR_934021.2:n.1489G>A | ||
| XR_934022.2:n.1489G>A | ||
| XR_934023.2:n.1489G>A | ||
| NM_000018.4:c.1430G>A MANE Select | NP_000009.1:p.Cys477Tyr | |
| NM_001033859.3:c.1364G>A | NP_001029031.1:p.Cys455Tyr | |
| NM_001270447.2:c.1499G>A | NP_001257376.1:p.Cys500Tyr | |
| NM_001270448.2:c.1202G>A | NP_001257377.1:p.Cys401Tyr |