Canonical Allele Identifier: CA2365869040

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651754C= , CM000682.2:g.44651754C=	GRCh38
NC_000020.10:g.43280395C= , CM000682.1:g.43280395C=	GRCh37
NC_000020.9:g.42713809C=	NCBI36
NG_007385.1:g.4982G= , LRG_16:g.4982G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-121+148G=	ENSP00000512234.1:n.-121+148G=
ENST00000696039.1:n.321+148G=
ENST00000696062.1:c.96+346G=	ENSP00000512365.1:n.96+346G=
ENST00000696064.1:c.-118+148G=	ENSP00000512367.1:n.-118+148G=
ENST00000696065.1:c.-121+148G=	ENSP00000512368.1:n.-121+148G=
ENST00000535573.1:n.332+148G=
ENST00000536076.1:n.213+148G=
XM_011528479.1:c.-257+148G=	XP_011526781.1:n.-257+148G=
NM_000022.3:c.-147G=	NP_000013.2:n.-147G=
NM_001322050.1:c.-436G=	NP_001308979.1:n.-436G=
NM_001322051.1:c.-147G=	NP_001308980.1:n.-147G=
NR_136160.1:n.5G=