Canonical Allele Identifier: CA212781
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790
ClinVar RCV Id: RCV000001863
dbSNP Id: rs786205061

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835249C>A , CM000672.2:g.102835249C>A GRCh38
NC_000010.10:g.104595006C>A , CM000672.1:g.104595006C>A GRCh37
NC_000010.9:g.104584996C>A NCBI36
NG_007955.1:g.7285G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.436+5G>T MANE Select ENSP00000358903.3:p.=
ENST00000638190.1:c.436+5G>T ENSP00000492539.1:p.=
ENST00000638272.1:c.297+1816G>T ENSP00000491508.1:p.=
ENST00000638971.1:c.436+5G>T ENSP00000492313.1:p.=
ENST00000639393.1:c.436+5G>T ENSP00000492651.1:p.=
ENST00000640633.1:n.198+5G>T
ENST00000369887.3:c.436+5G>T ENSP00000358903.3:p.=
ENST00000489268.1:n.690+5G>T
NM_000102.3:c.436+5G>T NP_000093.1:p.=
NM_000102.4:c.436+5G>T MANE Select NP_000093.1:p.=