Canonical Allele Identifier: CA2574654747

Gene: CYP17A1 WBP1L CYP17A1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832692_102832693del , CM000672.2:g.102832692_102832693del	GRCh38
NC_000010.10:g.104592449_104592450del , CM000672.1:g.104592449_104592450del	GRCh37
NC_000010.9:g.104582439_104582440del	NCBI36
NG_007955.1:g.9843_9844del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.970-11_970-10del (CYP17A1) MANE Select	ENSP00000358903.3:n.970-11_970-10del
ENST00000638190.1:c.667-11_667-10del (CYP17A1)	ENSP00000492539.1:n.667-11_667-10del
ENST00000638272.1:c.514-11_514-10del (CYP17A1)	ENSP00000491508.1:n.514-11_514-10del
ENST00000638971.1:c.883-11_883-10del (CYP17A1)	ENSP00000492313.1:n.883-11_883-10del
ENST00000639393.1:c.970-11_970-10del (CYP17A1)	ENSP00000492651.1:n.970-11_970-10del
ENST00000640633.1:n.732-11_732-10del (CYP17A1)
ENST00000647664.1:c.*1723_*1724del (WBP1L)	ENSP00000498131.1:n.*1723_*1724del
ENST00000369887.3:c.970-11_970-10del (CYP17A1)	ENSP00000358903.3:n.970-11_970-10del
NM_000102.3:c.970-11_970-10del (CYP17A1)	NP_000093.1:n.970-11_970-10del
XR_428804.1:n.26_27del (CYP17A1-AS1)
NM_000102.4:c.970-11_970-10del (CYP17A1) MANE Select	NP_000093.1:n.970-11_970-10del