Canonical Allele Identifier: CA1932873541

Gene: CYP17A1 CYP17A1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102833914_102833915delinsAC , CM000672.2:g.102833914_102833915delinsAC	GRCh38
NC_000010.10:g.104593671_104593672delinsAC , CM000672.1:g.104593671_104593672delinsAC	GRCh37
NC_000010.9:g.104583661_104583662delinsAC	NCBI36
NG_007955.1:g.8619_8620delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-263_152-262delinsAC
ENST00000369887.4:c.753+121_753+122delinsGT (CYP17A1) MANE Select	ENSP00000358903.3:n.753+121_753+122delinsGT
ENST00000638190.1:c.666+870_666+871delinsGT (CYP17A1)	ENSP00000492539.1:n.666+870_666+871delinsGT
ENST00000638272.1:c.298-707_298-706delinsGT (CYP17A1)	ENSP00000491508.1:n.298-707_298-706delinsGT
ENST00000638971.1:c.667-707_667-706delinsGT (CYP17A1)	ENSP00000492313.1:n.667-707_667-706delinsGT
ENST00000639393.1:c.753+121_753+122delinsGT (CYP17A1)	ENSP00000492651.1:n.753+121_753+122delinsGT
ENST00000640633.1:n.515+121_515+122delinsGT (CYP17A1)
ENST00000369887.3:c.753+121_753+122delinsGT (CYP17A1)	ENSP00000358903.3:n.753+121_753+122delinsGT
ENST00000489268.1:n.1790_1791delinsGT (CYP17A1)
NM_000102.3:c.753+121_753+122delinsGT (CYP17A1)	NP_000093.1:n.753+121_753+122delinsGT
XR_428804.1:n.206-263_206-262delinsAC (CYP17A1-AS1)
NM_000102.4:c.753+121_753+122delinsGT (CYP17A1) MANE Select	NP_000093.1:n.753+121_753+122delinsGT