Canonical Allele Identifier: CA377938516

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104591313G>T (hg19) ; chr10:g.102831556G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831556G>T , CM000672.2:g.102831556G>T	GRCh38
NC_000010.10:g.104591313G>T , CM000672.1:g.104591313G>T	GRCh37
NC_000010.9:g.104581303G>T	NCBI36
NG_007955.1:g.10978C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1195C>A (CYP17A1) MANE Select	ENSP00000358903.3:p.Leu399Met
ENST00000638190.1:c.892C>A (CYP17A1)	ENSP00000492539.1:p.Leu298Met
ENST00000638272.1:c.739C>A (CYP17A1)	ENSP00000491508.1:p.Leu247Met
ENST00000638971.1:c.1108C>A (CYP17A1)	ENSP00000492313.1:p.Leu370Met
ENST00000639393.1:c.1198C>A (CYP17A1)	ENSP00000492651.1:p.Leu400Met
ENST00000640633.1:n.957C>A (CYP17A1)
ENST00000647664.1:c.*629-42G>T (WBP1L)	ENSP00000498131.1:n.*629-42G>T
ENST00000369887.3:c.1195C>A (CYP17A1)	ENSP00000358903.3:p.Leu399Met
ENST00000469683.1:n.148C>A (CYP17A1)
NM_000102.3:c.1195C>A (CYP17A1)	NP_000093.1:p.Leu399Met
NM_000102.4:c.1195C>A (CYP17A1) MANE Select	NP_000093.1:p.Leu399Met