Canonical Allele Identifier: CA2610724533

Gene: CYP17A1

Linked Data

• gnomAD v4: 10-102835218-T-TCCAGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835229_102835234dup , CM000672.2:g.102835229_102835234dup	GRCh38
NC_000010.10:g.104594986_104594991dup , CM000672.1:g.104594986_104594991dup	GRCh37
NC_000010.9:g.104584976_104584981dup	NCBI36
NG_007955.1:g.7310_7315dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.436+30_436+35dup MANE Select	ENSP00000358903.3:n.436+30_436+35dup
ENST00000638190.1:c.436+30_436+35dup	ENSP00000492539.1:n.436+30_436+35dup
ENST00000638272.1:c.297+1841_297+1846dup	ENSP00000491508.1:n.297+1841_297+1846dup
ENST00000638971.1:c.436+30_436+35dup	ENSP00000492313.1:n.436+30_436+35dup
ENST00000639393.1:c.436+30_436+35dup	ENSP00000492651.1:n.436+30_436+35dup
ENST00000640633.1:n.198+30_198+35dup
ENST00000369887.3:c.436+30_436+35dup	ENSP00000358903.3:n.436+30_436+35dup
ENST00000489268.1:n.690+30_690+35dup
NM_000102.3:c.436+30_436+35dup	NP_000093.1:n.436+30_436+35dup
NM_000102.4:c.436+30_436+35dup MANE Select	NP_000093.1:n.436+30_436+35dup