Canonical Allele Identifier: CA471287949

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104591311C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831554C>A , CM000672.2:g.102831554C>A	GRCh38
NC_000010.10:g.104591311C>A , CM000672.1:g.104591311C>A	GRCh37
NC_000010.9:g.104581301C>A	NCBI36
NG_007955.1:g.10980G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1197G>T (CYP17A1) MANE Select	ENSP00000358903.3:p.Leu399=
ENST00000638190.1:c.894G>T (CYP17A1)	ENSP00000492539.1:p.Leu298=
ENST00000638272.1:c.741G>T (CYP17A1)	ENSP00000491508.1:p.Leu247=
ENST00000638971.1:c.1110G>T (CYP17A1)	ENSP00000492313.1:p.Leu370=
ENST00000639393.1:c.1200G>T (CYP17A1)	ENSP00000492651.1:p.Leu400=
ENST00000640633.1:n.959G>T (CYP17A1)
ENST00000647664.1:c.*629-44C>A (WBP1L)	ENSP00000498131.1:n.*629-44C>A
ENST00000369887.3:c.1197G>T (CYP17A1)	ENSP00000358903.3:p.Leu399=
ENST00000469683.1:n.150G>T (CYP17A1)
NM_000102.3:c.1197G>T (CYP17A1)	NP_000093.1:p.Leu399=
NM_000102.4:c.1197G>T (CYP17A1) MANE Select	NP_000093.1:p.Leu399=