Canonical Allele Identifier: CA2365869102

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651824A= , CM000682.2:g.44651824A=	GRCh38
NC_000020.10:g.43280465A= , CM000682.1:g.43280465A=	GRCh37
NC_000020.9:g.42713879A=	NCBI36
NG_007385.1:g.4912T= , LRG_16:g.4912T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-121+78T=	ENSP00000512234.1:n.-121+78T=
ENST00000696039.1:n.321+78T=
ENST00000696062.1:c.96+276T=	ENSP00000512365.1:n.96+276T=
ENST00000696064.1:c.-118+78T=	ENSP00000512367.1:n.-118+78T=
ENST00000696065.1:c.-121+78T=	ENSP00000512368.1:n.-121+78T=
ENST00000535573.1:n.332+78T=
ENST00000536076.1:n.213+78T=
XM_011528479.1:c.-257+78T=	XP_011526781.1:n.-257+78T=