Canonical Allele Identifier: CA377938427

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104591276T>C (hg19) ; chr10:g.102831519T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831519T>C , CM000672.2:g.102831519T>C	GRCh38
NC_000010.10:g.104591276T>C , CM000672.1:g.104591276T>C	GRCh37
NC_000010.9:g.104581266T>C	NCBI36
NG_007955.1:g.11015A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1232A>G (CYP17A1) MANE Select	ENSP00000358903.3:p.Gln411Arg
ENST00000638190.1:c.929A>G (CYP17A1)	ENSP00000492539.1:p.Gln310Arg
ENST00000638272.1:c.776A>G (CYP17A1)	ENSP00000491508.1:p.Gln259Arg
ENST00000638971.1:c.1145A>G (CYP17A1)	ENSP00000492313.1:p.Gln382Arg
ENST00000639393.1:c.1235A>G (CYP17A1)	ENSP00000492651.1:p.Gln412Arg
ENST00000640633.1:n.994A>G (CYP17A1)
ENST00000647664.1:c.*629-79T>C (WBP1L)	ENSP00000498131.1:n.*629-79T>C
ENST00000369887.3:c.1232A>G (CYP17A1)	ENSP00000358903.3:p.Gln411Arg
ENST00000469683.1:n.185A>G (CYP17A1)
NM_000102.3:c.1232A>G (CYP17A1)	NP_000093.1:p.Gln411Arg
NM_000102.4:c.1232A>G (CYP17A1) MANE Select	NP_000093.1:p.Gln411Arg