Canonical Allele Identifier: CA2652992669

Gene: ADA

Linked Data

• gnomAD v4: 20-44651907-G-GGC

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651914_44651915dup , CM000682.2:g.44651914_44651915dup	GRCh38
NC_000020.10:g.43280555_43280556dup , CM000682.1:g.43280555_43280556dup	GRCh37
NC_000020.9:g.42713969_42713970dup	NCBI36
NG_007385.1:g.4827_4828dup , LRG_16:g.4827_4828dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-128_-127dup	ENSP00000512234.1:n.-128_-127dup
ENST00000696039.1:n.314_315dup
ENST00000696062.1:c.96+191_96+192dup	ENSP00000512365.1:n.96+191_96+192dup
ENST00000696064.1:c.-125_-124dup	ENSP00000512367.1:n.-125_-124dup
ENST00000696065.1:c.-128_-127dup	ENSP00000512368.1:n.-128_-127dup
ENST00000535573.1:n.325_326dup
ENST00000536076.1:n.206_207dup
XM_011528479.1:c.-264_-263dup	XP_011526781.1:n.-264_-263dup