Canonical Allele Identifier: CA1932870829

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832662_102832663delinsCG , CM000672.2:g.102832662_102832663delinsCG	GRCh38
NC_000010.10:g.104592419_104592420delinsCG , CM000672.1:g.104592419_104592420delinsCG	GRCh37
NC_000010.9:g.104582409_104582410delinsCG	NCBI36
NG_007955.1:g.9871_9872delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.987_988delinsCG (CYP17A1) MANE Select	ENSP00000358903.3:p.Tyr329=
ENST00000638190.1:c.684_685delinsCG (CYP17A1)	ENSP00000492539.1:p.Tyr228=
ENST00000638272.1:c.531_532delinsCG (CYP17A1)	ENSP00000491508.1:p.Tyr177=
ENST00000638971.1:c.900_901delinsCG (CYP17A1)	ENSP00000492313.1:p.Tyr300=
ENST00000639393.1:c.987_988delinsCG (CYP17A1)	ENSP00000492651.1:p.Tyr329=
ENST00000640633.1:n.749_750delinsCG (CYP17A1)
ENST00000647664.1:c.*1693_*1694delinsCG (WBP1L)	ENSP00000498131.1:n.*1693_*1694delinsCG
ENST00000369887.3:c.987_988delinsCG (CYP17A1)	ENSP00000358903.3:p.Tyr329=
NM_000102.3:c.987_988delinsCG (CYP17A1)	NP_000093.1:p.Tyr329=
NM_000102.4:c.987_988delinsCG (CYP17A1) MANE Select	NP_000093.1:p.Tyr329=