Canonical Allele Identifier: CA2841925136

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832437_102832438insTG , CM000672.2:g.102832437_102832438insTG	GRCh38
NC_000010.10:g.104592194_104592195insTG , CM000672.1:g.104592194_104592195insTG	GRCh37
NC_000010.9:g.104582184_104582185insTG	NCBI36
NG_007955.1:g.10097_10098insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1139+74_1139+75insAC (CYP17A1) MANE Select	ENSP00000358903.3:n.1139+74_1139+75insAC
ENST00000638190.1:c.836+74_836+75insAC (CYP17A1)	ENSP00000492539.1:n.836+74_836+75insAC
ENST00000638272.1:c.683+74_683+75insAC (CYP17A1)	ENSP00000491508.1:n.683+74_683+75insAC
ENST00000638971.1:c.1052+74_1052+75insAC (CYP17A1)	ENSP00000492313.1:n.1052+74_1052+75insAC
ENST00000639393.1:c.1139+74_1139+75insAC (CYP17A1)	ENSP00000492651.1:n.1139+74_1139+75insAC
ENST00000640633.1:n.901+74_901+75insAC (CYP17A1)
ENST00000647664.1:c.*1468_*1469insTG (WBP1L)	ENSP00000498131.1:n.*1468_*1469insTG
ENST00000369887.3:c.1139+74_1139+75insAC (CYP17A1)	ENSP00000358903.3:n.1139+74_1139+75insAC
NM_000102.3:c.1139+74_1139+75insAC (CYP17A1)	NP_000093.1:n.1139+74_1139+75insAC
NM_000102.4:c.1139+74_1139+75insAC (CYP17A1) MANE Select	NP_000093.1:n.1139+74_1139+75insAC