Canonical Allele Identifier: CA2652992662

Gene: ADA

Linked Data

• gnomAD v4: 20-44651903-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651903T>G , CM000682.2:g.44651903T>G	GRCh38
NC_000020.10:g.43280544T>G , CM000682.1:g.43280544T>G	GRCh37
NC_000020.9:g.42713958T>G	NCBI36
NG_007385.1:g.4833A>C , LRG_16:g.4833A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-122A>C	ENSP00000512234.1:n.-122A>C
ENST00000696039.1:n.320A>C
ENST00000696062.1:c.96+197A>C	ENSP00000512365.1:n.96+197A>C
ENST00000696064.1:c.-119A>C	ENSP00000512367.1:n.-119A>C
ENST00000696065.1:c.-122A>C	ENSP00000512368.1:n.-122A>C
ENST00000535573.1:n.331A>C
ENST00000536076.1:n.212A>C
XM_011528479.1:c.-258A>C	XP_011526781.1:n.-258A>C