Canonical Allele Identifier: CA1932873822

Gene: CYP17A1 CYP17A1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834022_102834024delinsGCT , CM000672.2:g.102834022_102834024delinsGCT	GRCh38
NC_000010.10:g.104593779_104593781delinsGCT , CM000672.1:g.104593779_104593781delinsGCT	GRCh37
NC_000010.9:g.104583769_104583771delinsGCT	NCBI36
NG_007955.1:g.8510_8512delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-155_152-153delinsGCT
ENST00000369887.4:c.753+12_753+14delinsAGC (CYP17A1) MANE Select	ENSP00000358903.3:n.753+12_753+14delinsAGC
ENST00000638190.1:c.666+761_666+763delinsAGC (CYP17A1)	ENSP00000492539.1:n.666+761_666+763delinsAGC
ENST00000638272.1:c.298-816_298-814delinsAGC (CYP17A1)	ENSP00000491508.1:n.298-816_298-814delinsAGC
ENST00000638971.1:c.666+761_666+763delinsAGC (CYP17A1)	ENSP00000492313.1:n.666+761_666+763delinsAGC
ENST00000639393.1:c.753+12_753+14delinsAGC (CYP17A1)	ENSP00000492651.1:n.753+12_753+14delinsAGC
ENST00000640633.1:n.515+12_515+14delinsAGC (CYP17A1)
ENST00000369887.3:c.753+12_753+14delinsAGC (CYP17A1)	ENSP00000358903.3:n.753+12_753+14delinsAGC
ENST00000489268.1:n.1681_1683delinsAGC (CYP17A1)
NM_000102.3:c.753+12_753+14delinsAGC (CYP17A1)	NP_000093.1:n.753+12_753+14delinsAGC
XR_428804.1:n.206-155_206-153delinsGCT (CYP17A1-AS1)
NM_000102.4:c.753+12_753+14delinsAGC (CYP17A1) MANE Select	NP_000093.1:n.753+12_753+14delinsAGC