Canonical Allele Identifier: CA2652992656

Gene: ADA

Linked Data

• gnomAD v4: 20-44651895-G-GTC

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651895_44651896insTC , CM000682.2:g.44651895_44651896insTC	GRCh38
NC_000020.10:g.43280536_43280537insTC , CM000682.1:g.43280536_43280537insTC	GRCh37
NC_000020.9:g.42713950_42713951insTC	NCBI36
NG_007385.1:g.4840_4841insGA , LRG_16:g.4840_4841insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-121+6_-121+7insGA	ENSP00000512234.1:n.-121+6_-121+7insGA
ENST00000696039.1:n.321+6_321+7insGA
ENST00000696062.1:c.96+204_96+205insGA	ENSP00000512365.1:n.96+204_96+205insGA
ENST00000696064.1:c.-118+6_-118+7insGA	ENSP00000512367.1:n.-118+6_-118+7insGA
ENST00000696065.1:c.-121+6_-121+7insGA	ENSP00000512368.1:n.-121+6_-121+7insGA
ENST00000535573.1:n.332+6_332+7insGA
ENST00000536076.1:n.213+6_213+7insGA
XM_011528479.1:c.-257+6_-257+7insGA	XP_011526781.1:n.-257+6_-257+7insGA