Canonical Allele Identifier: CA377938682

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102832524-T-C
• MyVariant Identifiers: chr10:g.104592281T>C (hg19) ; chr10:g.102832524T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832524T>C , CM000672.2:g.102832524T>C	GRCh38
NC_000010.10:g.104592281T>C , CM000672.1:g.104592281T>C	GRCh37
NC_000010.9:g.104582271T>C	NCBI36
NG_007955.1:g.10010A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1126A>G (CYP17A1) MANE Select	ENSP00000358903.3:p.Asn376Asp
ENST00000638190.1:c.823A>G (CYP17A1)	ENSP00000492539.1:p.Asn275Asp
ENST00000638272.1:c.670A>G (CYP17A1)	ENSP00000491508.1:p.Asn224Asp
ENST00000638971.1:c.1039A>G (CYP17A1)	ENSP00000492313.1:p.Asn347Asp
ENST00000639393.1:c.1126A>G (CYP17A1)	ENSP00000492651.1:p.Asn376Asp
ENST00000640633.1:n.888A>G (CYP17A1)
ENST00000647664.1:c.*1555T>C (WBP1L)	ENSP00000498131.1:n.*1555T>C
ENST00000369887.3:c.1126A>G (CYP17A1)	ENSP00000358903.3:p.Asn376Asp
NM_000102.3:c.1126A>G (CYP17A1)	NP_000093.1:p.Asn376Asp
NM_000102.4:c.1126A>G (CYP17A1) MANE Select	NP_000093.1:p.Asn376Asp