Canonical Allele Identifier: CA2652992709

Gene: ADA

Linked Data

• gnomAD v4: 20-44651942-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651948del , CM000682.2:g.44651948del	GRCh38
NC_000020.10:g.43280589del , CM000682.1:g.43280589del	GRCh37
NC_000020.9:g.42714003del	NCBI36
NG_007385.1:g.4793del , LRG_16:g.4793del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-162del	ENSP00000512234.1:n.-162del
ENST00000696039.1:n.280del
ENST00000696062.1:c.96+157del	ENSP00000512365.1:n.96+157del
ENST00000696064.1:c.-159del	ENSP00000512367.1:n.-159del
ENST00000535573.1:n.291del
ENST00000536076.1:n.172del
XM_011528479.1:c.-298del	XP_011526781.1:n.-298del