Canonical Allele Identifier: CA2365869116

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651847C= , CM000682.2:g.44651847C=	GRCh38
NC_000020.10:g.43280488C= , CM000682.1:g.43280488C=	GRCh37
NC_000020.9:g.42713902C=	NCBI36
NG_007385.1:g.4889G= , LRG_16:g.4889G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-121+55G=	ENSP00000512234.1:n.-121+55G=
ENST00000696039.1:n.321+55G=
ENST00000696062.1:c.96+253G=	ENSP00000512365.1:n.96+253G=
ENST00000696064.1:c.-118+55G=	ENSP00000512367.1:n.-118+55G=
ENST00000696065.1:c.-121+55G=	ENSP00000512368.1:n.-121+55G=
ENST00000535573.1:n.332+55G=
ENST00000536076.1:n.213+55G=
XM_011528479.1:c.-257+55G=	XP_011526781.1:n.-257+55G=