Canonical Allele Identifier: CA5669669
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 298628
ClinVar RCV Id: RCV000267824
dbSNP Id: rs140012815

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837376G>A , CM000672.2:g.102837376G>A GRCh38
NC_000010.10:g.104597133G>A , CM000672.1:g.104597133G>A GRCh37
NC_000010.9:g.104587123G>A NCBI36
NG_007955.1:g.5158C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.-15C>T MANE Select ENSP00000358903.3:n.-15C>T
ENST00000638190.1:c.-15C>T ENSP00000492539.1:n.-15C>T
ENST00000638272.1:c.-15C>T ENSP00000491508.1:n.-15C>T
ENST00000638971.1:c.-15C>T ENSP00000492313.1:n.-15C>T
ENST00000639393.1:c.-15C>T ENSP00000492651.1:n.-15C>T
ENST00000369887.3:c.-15C>T ENSP00000358903.3:n.-15C>T
ENST00000489268.1:n.39C>T
NM_000102.3:c.-15C>T NP_000093.1:n.-15C>T
NM_000102.4:c.-15C>T MANE Select NP_000093.1:n.-15C>T