Canonical Allele Identifier: CA2789273577

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835192_102835194del , CM000672.2:g.102835192_102835194del	GRCh38
NC_000010.10:g.104594949_104594951del , CM000672.1:g.104594949_104594951del	GRCh37
NC_000010.9:g.104584939_104584941del	NCBI36
NG_007955.1:g.7344_7346del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.436+64_436+66del MANE Select	ENSP00000358903.3:n.436+64_436+66del
ENST00000638190.1:c.436+64_436+66del	ENSP00000492539.1:n.436+64_436+66del
ENST00000638272.1:c.297+1875_297+1877del	ENSP00000491508.1:n.297+1875_297+1877del
ENST00000638971.1:c.436+64_436+66del	ENSP00000492313.1:n.436+64_436+66del
ENST00000639393.1:c.436+64_436+66del	ENSP00000492651.1:n.436+64_436+66del
ENST00000640633.1:n.198+64_198+66del
ENST00000369887.3:c.436+64_436+66del	ENSP00000358903.3:n.436+64_436+66del
ENST00000489268.1:n.690+64_690+66del
NM_000102.3:c.436+64_436+66del	NP_000093.1:n.436+64_436+66del
NM_000102.4:c.436+64_436+66del MANE Select	NP_000093.1:n.436+64_436+66del