Canonical Allele Identifier: CA2610724530

Gene: CYP17A1

Linked Data

• gnomAD v4: 10-102835215-G-GGATCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835217_102835222dup , CM000672.2:g.102835217_102835222dup	GRCh38
NC_000010.10:g.104594974_104594979dup , CM000672.1:g.104594974_104594979dup	GRCh37
NC_000010.9:g.104584964_104584969dup	NCBI36
NG_007955.1:g.7313_7318dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.436+33_436+38dup MANE Select	ENSP00000358903.3:n.436+33_436+38dup
ENST00000638190.1:c.436+33_436+38dup	ENSP00000492539.1:n.436+33_436+38dup
ENST00000638272.1:c.297+1844_297+1849dup	ENSP00000491508.1:n.297+1844_297+1849dup
ENST00000638971.1:c.436+33_436+38dup	ENSP00000492313.1:n.436+33_436+38dup
ENST00000639393.1:c.436+33_436+38dup	ENSP00000492651.1:n.436+33_436+38dup
ENST00000640633.1:n.198+33_198+38dup
ENST00000369887.3:c.436+33_436+38dup	ENSP00000358903.3:n.436+33_436+38dup
ENST00000489268.1:n.690+33_690+38dup
NM_000102.3:c.436+33_436+38dup	NP_000093.1:n.436+33_436+38dup
NM_000102.4:c.436+33_436+38dup MANE Select	NP_000093.1:n.436+33_436+38dup