Canonical Allele Identifier: CA1932839514

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835235_102835244delinsGGGCCAGCCT , CM000672.2:g.102835235_102835244delinsGGGCCAGCCT	GRCh38
NC_000010.10:g.104594992_104595001delinsGGGCCAGCCT , CM000672.1:g.104594992_104595001delinsGGGCCAGCCT	GRCh37
NC_000010.9:g.104584982_104584991delinsGGGCCAGCCT	NCBI36
NG_007955.1:g.7290_7299delinsAGGCTGGCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.436+10_436+19delinsAGGCTGGCCC MANE Select	ENSP00000358903.3:n.436+10_436+19delinsAG...
ENST00000638190.1:c.436+10_436+19delinsAGGCTGGCCC	ENSP00000492539.1:n.436+10_436+19delinsAG...
ENST00000638272.1:c.297+1821_297+1830delinsAGGCTGGCCC	ENSP00000491508.1:n.297+1821_297+1830deli...
ENST00000638971.1:c.436+10_436+19delinsAGGCTGGCCC	ENSP00000492313.1:n.436+10_436+19delinsAG...
ENST00000639393.1:c.436+10_436+19delinsAGGCTGGCCC	ENSP00000492651.1:n.436+10_436+19delinsAG...
ENST00000640633.1:n.198+10_198+19delinsAGGCTGGCCC
ENST00000369887.3:c.436+10_436+19delinsAGGCTGGCCC	ENSP00000358903.3:n.436+10_436+19delinsAG...
ENST00000489268.1:n.690+10_690+19delinsAGGCTGGCCC
NM_000102.3:c.436+10_436+19delinsAGGCTGGCCC	NP_000093.1:n.436+10_436+19delinsAGGCTGGC...
NM_000102.4:c.436+10_436+19delinsAGGCTGGCCC MANE Select	NP_000093.1:n.436+10_436+19delinsAGGCTGGC...