Canonical Allele Identifier: CA2610723713

Gene: CYP17A1 WBP1L CYP17A1-AS1

Linked Data

• gnomAD v4: 10-102833621-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833621T>C , CM000672.2:g.102833621T>C	GRCh38
NC_000010.10:g.104593378T>C , CM000672.1:g.104593378T>C	GRCh37
NC_000010.9:g.104583368T>C	NCBI36
NG_007955.1:g.8913A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-556T>C
ENST00000369887.4:c.754-413A>G (CYP17A1) MANE Select	ENSP00000358903.3:n.754-413A>G
ENST00000638190.1:c.667-941A>G (CYP17A1)	ENSP00000492539.1:n.667-941A>G
ENST00000638272.1:c.298-413A>G (CYP17A1)	ENSP00000491508.1:n.298-413A>G
ENST00000638971.1:c.667-413A>G (CYP17A1)	ENSP00000492313.1:n.667-413A>G
ENST00000639393.1:c.754-413A>G (CYP17A1)	ENSP00000492651.1:n.754-413A>G
ENST00000640633.1:n.516-413A>G (CYP17A1)
ENST00000647664.1:c.*2652T>C (WBP1L)	ENSP00000498131.1:n.*2652T>C
ENST00000369887.3:c.754-413A>G (CYP17A1)	ENSP00000358903.3:n.754-413A>G
ENST00000489268.1:n.2084A>G (CYP17A1)
NM_000102.3:c.754-413A>G (CYP17A1)	NP_000093.1:n.754-413A>G
XR_428804.1:n.206-556T>C (CYP17A1-AS1)
NM_000102.4:c.754-413A>G (CYP17A1) MANE Select	NP_000093.1:n.754-413A>G