Canonical Allele Identifier: CA1932867113

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830897_102830898delinsAC , CM000672.2:g.102830897_102830898delinsAC	GRCh38
NC_000010.10:g.104590654_104590655delinsAC , CM000672.1:g.104590654_104590655delinsAC	GRCh37
NC_000010.9:g.104580644_104580645delinsAC	NCBI36
NG_007955.1:g.11636_11637delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1331_1332delinsGT (CYP17A1) MANE Select	ENSP00000358903.3:p.Gly444=
ENST00000638190.1:c.1028_1029delinsGT (CYP17A1)	ENSP00000492539.1:p.Gly343=
ENST00000638272.1:c.875_876delinsGT (CYP17A1)	ENSP00000491508.1:p.Gly292=
ENST00000638971.1:c.1244_1245delinsGT (CYP17A1)	ENSP00000492313.1:p.Gly415=
ENST00000639393.1:c.1334_1335delinsGT (CYP17A1)	ENSP00000492651.1:p.Gly445=
ENST00000640633.1:n.1093_1094delinsGT (CYP17A1)
ENST00000647664.1:c.*579_*580delinsAC (WBP1L)	ENSP00000498131.1:n.*579_*580delinsAC
ENST00000369887.3:c.1331_1332delinsGT (CYP17A1)	ENSP00000358903.3:p.Gly444=
NM_000102.3:c.1331_1332delinsGT (CYP17A1)	NP_000093.1:p.Gly444=
NM_000102.4:c.1331_1332delinsGT (CYP17A1) MANE Select	NP_000093.1:p.Gly444=