Canonical Allele Identifier: CA1932839728
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2757019
ClinVar RCV Id: RCV003567056
dbSNP Id: rs1564779218

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835402G>A , CM000672.2:g.102835402G>A GRCh38
NC_000010.10:g.104595159G>A , CM000672.1:g.104595159G>A GRCh37
NC_000010.9:g.104585149G>A NCBI36
NG_007955.1:g.7132C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.298-10C>T MANE Select ENSP00000358903.3:n.298-10C>T
ENST00000638190.1:c.298-10C>T ENSP00000492539.1:n.298-10C>T
ENST00000638272.1:c.297+1663C>T ENSP00000491508.1:n.297+1663C>T
ENST00000638971.1:c.298-10C>T ENSP00000492313.1:n.298-10C>T
ENST00000639393.1:c.298-10C>T ENSP00000492651.1:n.298-10C>T
ENST00000640633.1:n.60-10C>T
ENST00000369887.3:c.298-10C>T ENSP00000358903.3:n.298-10C>T
ENST00000489268.1:n.542C>T
NM_000102.3:c.298-10C>T NP_000093.1:n.298-10C>T
NM_000102.4:c.298-10C>T MANE Select NP_000093.1:n.298-10C>T