Canonical Allele Identifier: CA377938400

Gene: CYP17A1 WBP1L

Linked Data

• dbSNP Id: rs1844088267
• gnomAD v4: 10-102831508-C-G
• MyVariant Identifiers: chr10:g.104591265C>G (hg19) ; chr10:g.102831508C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831508C>G , CM000672.2:g.102831508C>G	GRCh38
NC_000010.10:g.104591265C>G , CM000672.1:g.104591265C>G	GRCh37
NC_000010.9:g.104581255C>G	NCBI36
NG_007955.1:g.11026G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1243G>C (CYP17A1) MANE Select	ENSP00000358903.3:p.Glu415Gln
ENST00000638190.1:c.940G>C (CYP17A1)	ENSP00000492539.1:p.Glu314Gln
ENST00000638272.1:c.787G>C (CYP17A1)	ENSP00000491508.1:p.Glu263Gln
ENST00000638971.1:c.1156G>C (CYP17A1)	ENSP00000492313.1:p.Glu386Gln
ENST00000639393.1:c.1246G>C (CYP17A1)	ENSP00000492651.1:p.Glu416Gln
ENST00000640633.1:n.1005G>C (CYP17A1)
ENST00000647664.1:c.*629-90C>G (WBP1L)	ENSP00000498131.1:n.*629-90C>G
ENST00000369887.3:c.1243G>C (CYP17A1)	ENSP00000358903.3:p.Glu415Gln
ENST00000469683.1:n.196G>C (CYP17A1)
NM_000102.3:c.1243G>C (CYP17A1)	NP_000093.1:p.Glu415Gln
NM_000102.4:c.1243G>C (CYP17A1) MANE Select	NP_000093.1:p.Glu415Gln