Canonical Allele Identifier: CA2652992666

Gene: ADA

Linked Data

• gnomAD v4: 20-44651905-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651908del , CM000682.2:g.44651908del	GRCh38
NC_000020.10:g.43280549del , CM000682.1:g.43280549del	GRCh37
NC_000020.9:g.42713963del	NCBI36
NG_007385.1:g.4830del , LRG_16:g.4830del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-125del	ENSP00000512234.1:n.-125del
ENST00000696039.1:n.317del
ENST00000696062.1:c.96+194del	ENSP00000512365.1:n.96+194del
ENST00000696064.1:c.-122del	ENSP00000512367.1:n.-122del
ENST00000696065.1:c.-125del	ENSP00000512368.1:n.-125del
ENST00000535573.1:n.328del
ENST00000536076.1:n.209del
XM_011528479.1:c.-261del	XP_011526781.1:n.-261del