Canonical Allele Identifier: CA2610723751

Gene: CYP17A1 WBP1L CYP17A1-AS1

Linked Data

• gnomAD v4: 10-102833673-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833673C>T , CM000672.2:g.102833673C>T	GRCh38
NC_000010.10:g.104593430C>T , CM000672.1:g.104593430C>T	GRCh37
NC_000010.9:g.104583420C>T	NCBI36
NG_007955.1:g.8861G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-504C>T
ENST00000369887.4:c.753+363G>A (CYP17A1) MANE Select	ENSP00000358903.3:n.753+363G>A
ENST00000638190.1:c.667-993G>A (CYP17A1)	ENSP00000492539.1:n.667-993G>A
ENST00000638272.1:c.298-465G>A (CYP17A1)	ENSP00000491508.1:n.298-465G>A
ENST00000638971.1:c.667-465G>A (CYP17A1)	ENSP00000492313.1:n.667-465G>A
ENST00000639393.1:c.753+363G>A (CYP17A1)	ENSP00000492651.1:n.753+363G>A
ENST00000640633.1:n.515+363G>A (CYP17A1)
ENST00000647664.1:c.*2704C>T (WBP1L)	ENSP00000498131.1:n.*2704C>T
ENST00000369887.3:c.753+363G>A (CYP17A1)	ENSP00000358903.3:n.753+363G>A
ENST00000489268.1:n.2032G>A (CYP17A1)
NM_000102.3:c.753+363G>A (CYP17A1)	NP_000093.1:n.753+363G>A
XR_428804.1:n.206-504C>T (CYP17A1-AS1)
NM_000102.4:c.753+363G>A (CYP17A1) MANE Select	NP_000093.1:n.753+363G>A