Canonical Allele Identifier: CA471288100

Gene: CYP17A1 WBP1L

Linked Data

• ClinVar Variation Id: 2024520
• ClinVar RCV Id: RCV002847752
• MyVariant Identifiers: chr10:g.104591362A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831605A>C , CM000672.2:g.102831605A>C	GRCh38
NC_000010.10:g.104591362A>C , CM000672.1:g.104591362A>C	GRCh37
NC_000010.9:g.104581352A>C	NCBI36
NG_007955.1:g.10929T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1146T>G (CYP17A1) MANE Select	ENSP00000358903.3:p.Gly382=
ENST00000638190.1:c.843T>G (CYP17A1)	ENSP00000492539.1:p.Gly281=
ENST00000638272.1:c.690T>G (CYP17A1)	ENSP00000491508.1:p.Gly230=
ENST00000638971.1:c.1059T>G (CYP17A1)	ENSP00000492313.1:p.Gly353=
ENST00000639393.1:c.1149T>G (CYP17A1)	ENSP00000492651.1:p.Gly383=
ENST00000640633.1:n.908T>G (CYP17A1)
ENST00000647664.1:c.*636A>C (WBP1L)	ENSP00000498131.1:n.*636A>C
ENST00000369887.3:c.1146T>G (CYP17A1)	ENSP00000358903.3:p.Gly382=
ENST00000469683.1:n.99T>G (CYP17A1)
NM_000102.3:c.1146T>G (CYP17A1)	NP_000093.1:p.Gly382=
NM_000102.4:c.1146T>G (CYP17A1) MANE Select	NP_000093.1:p.Gly382=