Canonical Allele Identifier: CA377938386

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104590742T>A (hg19) ; chr10:g.102830985T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830985T>A , CM000672.2:g.102830985T>A	GRCh38
NC_000010.10:g.104590742T>A , CM000672.1:g.104590742T>A	GRCh37
NC_000010.9:g.104580732T>A	NCBI36
NG_007955.1:g.11549A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1244A>T (CYP17A1) MANE Select	ENSP00000358903.3:p.Glu415Val
ENST00000638190.1:c.941A>T (CYP17A1)	ENSP00000492539.1:p.Glu314Val
ENST00000638272.1:c.788A>T (CYP17A1)	ENSP00000491508.1:p.Glu263Val
ENST00000638971.1:c.1157A>T (CYP17A1)	ENSP00000492313.1:p.Glu386Val
ENST00000639393.1:c.1247A>T (CYP17A1)	ENSP00000492651.1:p.Glu416Val
ENST00000640633.1:n.1006A>T (CYP17A1)
ENST00000647664.1:c.*628+39T>A (WBP1L)	ENSP00000498131.1:n.*628+39T>A
ENST00000369887.3:c.1244A>T (CYP17A1)	ENSP00000358903.3:p.Glu415Val
ENST00000469683.1:n.197A>T (CYP17A1)
NM_000102.3:c.1244A>T (CYP17A1)	NP_000093.1:p.Glu415Val
NM_000102.4:c.1244A>T (CYP17A1) MANE Select	NP_000093.1:p.Glu415Val