Canonical Allele Identifier: CA2610723758

Gene: CYP17A1 WBP1L CYP17A1-AS1

Linked Data

• gnomAD v4: 10-102833679-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833679C>A , CM000672.2:g.102833679C>A	GRCh38
NC_000010.10:g.104593436C>A , CM000672.1:g.104593436C>A	GRCh37
NC_000010.9:g.104583426C>A	NCBI36
NG_007955.1:g.8855G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-498C>A
ENST00000369887.4:c.753+357G>T (CYP17A1) MANE Select	ENSP00000358903.3:n.753+357G>T
ENST00000638190.1:c.667-999G>T (CYP17A1)	ENSP00000492539.1:n.667-999G>T
ENST00000638272.1:c.298-471G>T (CYP17A1)	ENSP00000491508.1:n.298-471G>T
ENST00000638971.1:c.667-471G>T (CYP17A1)	ENSP00000492313.1:n.667-471G>T
ENST00000639393.1:c.753+357G>T (CYP17A1)	ENSP00000492651.1:n.753+357G>T
ENST00000640633.1:n.515+357G>T (CYP17A1)
ENST00000647664.1:c.*2710C>A (WBP1L)	ENSP00000498131.1:n.*2710C>A
ENST00000369887.3:c.753+357G>T (CYP17A1)	ENSP00000358903.3:n.753+357G>T
ENST00000489268.1:n.2026G>T (CYP17A1)
NM_000102.3:c.753+357G>T (CYP17A1)	NP_000093.1:n.753+357G>T
XR_428804.1:n.206-498C>A (CYP17A1-AS1)
NM_000102.4:c.753+357G>T (CYP17A1) MANE Select	NP_000093.1:n.753+357G>T