Canonical Allele Identifier: CA377939891

Gene: CYP17A1

Linked Data

• MyVariant Identifiers: chr10:g.104594619C>A (hg19) ; chr10:g.102834862C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834862C>A , CM000672.2:g.102834862C>A	GRCh38
NC_000010.10:g.104594619C>A , CM000672.1:g.104594619C>A	GRCh37
NC_000010.9:g.104584609C>A	NCBI36
NG_007955.1:g.7672G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.589G>T MANE Select	ENSP00000358903.3:p.Val197Phe
ENST00000638190.1:c.589G>T	ENSP00000492539.1:p.Val197Phe
ENST00000638272.1:c.298-1654G>T	ENSP00000491508.1:n.298-1654G>T
ENST00000638971.1:c.589G>T	ENSP00000492313.1:p.Val197Phe
ENST00000639393.1:c.589G>T	ENSP00000492651.1:p.Val197Phe
ENST00000640633.1:n.351G>T
ENST00000369887.3:c.589G>T	ENSP00000358903.3:p.Val197Phe
ENST00000489268.1:n.843G>T
NM_000102.3:c.589G>T	NP_000093.1:p.Val197Phe
NM_000102.4:c.589G>T MANE Select	NP_000093.1:p.Val197Phe