Canonical Allele Identifier: CA377938667

Gene: CYP17A1 WBP1L

Linked Data

• dbSNP Id: rs1564778081
• gnomAD v4: 10-102832517-T-G
• MyVariant Identifiers: chr10:g.104592274T>G (hg19) ; chr10:g.102832517T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832517T>G , CM000672.2:g.102832517T>G	GRCh38
NC_000010.10:g.104592274T>G , CM000672.1:g.104592274T>G	GRCh37
NC_000010.9:g.104582264T>G	NCBI36
NG_007955.1:g.10017A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1133A>C (CYP17A1) MANE Select	ENSP00000358903.3:p.Asp378Ala
ENST00000638190.1:c.830A>C (CYP17A1)	ENSP00000492539.1:p.Asp277Ala
ENST00000638272.1:c.677A>C (CYP17A1)	ENSP00000491508.1:p.Asp226Ala
ENST00000638971.1:c.1046A>C (CYP17A1)	ENSP00000492313.1:p.Asp349Ala
ENST00000639393.1:c.1133A>C (CYP17A1)	ENSP00000492651.1:p.Asp378Ala
ENST00000640633.1:n.895A>C (CYP17A1)
ENST00000647664.1:c.*1548T>G (WBP1L)	ENSP00000498131.1:n.*1548T>G
ENST00000369887.3:c.1133A>C (CYP17A1)	ENSP00000358903.3:p.Asp378Ala
NM_000102.3:c.1133A>C (CYP17A1)	NP_000093.1:p.Asp378Ala
NM_000102.4:c.1133A>C (CYP17A1) MANE Select	NP_000093.1:p.Asp378Ala