Canonical Allele Identifier: CA2365869201

Gene: ADA

Linked Data

• dbSNP Id: rs2065652747

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651986_44651987del , CM000682.2:g.44651986_44651987del	GRCh38
NC_000020.10:g.43280627_43280628del , CM000682.1:g.43280627_43280628del	GRCh37
NC_000020.9:g.42714041_42714042del	NCBI36
NG_007385.1:g.4749_4750del , LRG_16:g.4749_4750del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-206_-205del	ENSP00000512234.1:n.-206_-205del
ENST00000696039.1:n.236_237del
ENST00000696062.1:c.96+113_96+114del	ENSP00000512365.1:n.96+113_96+114del
ENST00000696064.1:c.-203_-202del	ENSP00000512367.1:n.-203_-202del
ENST00000535573.1:n.247_248del
ENST00000536076.1:n.128_129del
XM_011528479.1:c.-342_-341del	XP_011526781.1:n.-342_-341del