Canonical Allele Identifier: CA2652992692

Gene: ADA

Linked Data

• gnomAD v4: 20-44651928-GCTGGGCGCTGCCTTCCCCCCGGCTCCTCCAGCAACTTTCAAGCGTCCCCCTGCAGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651940_44651995del , CM000682.2:g.44651940_44651995del	GRCh38
NC_000020.10:g.43280581_43280636del , CM000682.1:g.43280581_43280636del	GRCh37
NC_000020.9:g.42713995_42714050del	NCBI36
NG_007385.1:g.4752_4807del , LRG_16:g.4752_4807del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-203_-148del	ENSP00000512234.1:n.-203_-148del
ENST00000696039.1:n.239_294del
ENST00000696062.1:c.96+116_96+171del	ENSP00000512365.1:n.96+116_96+171del
ENST00000696064.1:c.-200_-145del	ENSP00000512367.1:n.-200_-145del
ENST00000535573.1:n.250_305del
ENST00000536076.1:n.131_186del
XM_011528479.1:c.-339_-284del	XP_011526781.1:n.-339_-284del