Canonical Allele Identifier: CA1932870188

Gene: CYP17A1 WBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832429_102832430delinsCG , CM000672.2:g.102832429_102832430delinsCG	GRCh38
NC_000010.10:g.104592186_104592187delinsCG , CM000672.1:g.104592186_104592187delinsCG	GRCh37
NC_000010.9:g.104582176_104582177delinsCG	NCBI36
NG_007955.1:g.10104_10105delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1139+81_1139+82delinsCG (CYP17A1) MANE Select	ENSP00000358903.3:n.1139+81_1139+82delins...
ENST00000638190.1:c.836+81_836+82delinsCG (CYP17A1)	ENSP00000492539.1:n.836+81_836+82delinsCG...
ENST00000638272.1:c.683+81_683+82delinsCG (CYP17A1)	ENSP00000491508.1:n.683+81_683+82delinsCG...
ENST00000638971.1:c.1052+81_1052+82delinsCG (CYP17A1)	ENSP00000492313.1:n.1052+81_1052+82delins...
ENST00000639393.1:c.1139+81_1139+82delinsCG (CYP17A1)	ENSP00000492651.1:n.1139+81_1139+82delins...
ENST00000640633.1:n.901+81_901+82delinsCG (CYP17A1)
ENST00000647664.1:c.*1460_*1461delinsCG (WBP1L)	ENSP00000498131.1:n.*1460_*1461delinsCG
ENST00000369887.3:c.1139+81_1139+82delinsCG (CYP17A1)	ENSP00000358903.3:n.1139+81_1139+82delins...
NM_000102.3:c.1139+81_1139+82delinsCG (CYP17A1)	NP_000093.1:n.1139+81_1139+82delinsCG
NM_000102.4:c.1139+81_1139+82delinsCG (CYP17A1) MANE Select	NP_000093.1:n.1139+81_1139+82delinsCG