Canonical Allele Identifier: CA2652992705

Gene: ADA

Linked Data

• gnomAD v4: 20-44651940-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651942del , CM000682.2:g.44651942del	GRCh38
NC_000020.10:g.43280583del , CM000682.1:g.43280583del	GRCh37
NC_000020.9:g.42713997del	NCBI36
NG_007385.1:g.4795del , LRG_16:g.4795del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-160del	ENSP00000512234.1:n.-160del
ENST00000696039.1:n.282del
ENST00000696062.1:c.96+159del	ENSP00000512365.1:n.96+159del
ENST00000696064.1:c.-157del	ENSP00000512367.1:n.-157del
ENST00000535573.1:n.293del
ENST00000536076.1:n.174del
XM_011528479.1:c.-296del	XP_011526781.1:n.-296del