Canonical Allele Identifier: CA2652992719

Gene: ADA

Linked Data

• gnomAD v4: 20-44651952-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651954del , CM000682.2:g.44651954del	GRCh38
NC_000020.10:g.43280595del , CM000682.1:g.43280595del	GRCh37
NC_000020.9:g.42714009del	NCBI36
NG_007385.1:g.4783del , LRG_16:g.4783del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-172del	ENSP00000512234.1:n.-172del
ENST00000696039.1:n.270del
ENST00000696062.1:c.96+147del	ENSP00000512365.1:n.96+147del
ENST00000696064.1:c.-169del	ENSP00000512367.1:n.-169del
ENST00000535573.1:n.281del
ENST00000536076.1:n.162del
XM_011528479.1:c.-308del	XP_011526781.1:n.-308del