Canonical Allele Identifier: CA2610723188

Gene: CYP17A1 WBP1L

Linked Data

• dbSNP Id: rs2134082258
• gnomAD v4: 10-102832467-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832467T>C , CM000672.2:g.102832467T>C	GRCh38
NC_000010.10:g.104592224T>C , CM000672.1:g.104592224T>C	GRCh37
NC_000010.9:g.104582214T>C	NCBI36
NG_007955.1:g.10067A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1139+44A>G (CYP17A1) MANE Select	ENSP00000358903.3:n.1139+44A>G
ENST00000638190.1:c.836+44A>G (CYP17A1)	ENSP00000492539.1:n.836+44A>G
ENST00000638272.1:c.683+44A>G (CYP17A1)	ENSP00000491508.1:n.683+44A>G
ENST00000638971.1:c.1052+44A>G (CYP17A1)	ENSP00000492313.1:n.1052+44A>G
ENST00000639393.1:c.1139+44A>G (CYP17A1)	ENSP00000492651.1:n.1139+44A>G
ENST00000640633.1:n.901+44A>G (CYP17A1)
ENST00000647664.1:c.*1498T>C (WBP1L)	ENSP00000498131.1:n.*1498T>C
ENST00000369887.3:c.1139+44A>G (CYP17A1)	ENSP00000358903.3:n.1139+44A>G
NM_000102.3:c.1139+44A>G (CYP17A1)	NP_000093.1:n.1139+44A>G
NM_000102.4:c.1139+44A>G (CYP17A1) MANE Select	NP_000093.1:n.1139+44A>G