Canonical Allele Identifier: CA3003424029

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835226del , CM000672.2:g.102835226del	GRCh38
NC_000010.10:g.104594983del , CM000672.1:g.104594983del	GRCh37
NC_000010.9:g.104584973del	NCBI36
NG_007955.1:g.7311del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.436+31del MANE Select	ENSP00000358903.3:n.436+31del
ENST00000638190.1:c.436+31del	ENSP00000492539.1:n.436+31del
ENST00000638272.1:c.297+1842del	ENSP00000491508.1:n.297+1842del
ENST00000638971.1:c.436+31del	ENSP00000492313.1:n.436+31del
ENST00000639393.1:c.436+31del	ENSP00000492651.1:n.436+31del
ENST00000640633.1:n.198+31del
ENST00000369887.3:c.436+31del	ENSP00000358903.3:n.436+31del
ENST00000489268.1:n.690+31del
NM_000102.3:c.436+31del	NP_000093.1:n.436+31del
NM_000102.4:c.436+31del MANE Select	NP_000093.1:n.436+31del