Canonical Allele Identifier: CA2365869002

Gene: ADA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651711C= , CM000682.2:g.44651711C=	GRCh38
NC_000020.10:g.43280352C= , CM000682.1:g.43280352C=	GRCh37
NC_000020.9:g.42713766C=	NCBI36
NG_007385.1:g.5025G= , LRG_16:g.5025G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-121+191G=	ENSP00000512234.1:n.-121+191G=
ENST00000537820.2:c.-104G=	ENSP00000441818.1:n.-104G=
ENST00000695949.1:c.-104G=	ENSP00000512281.1:n.-104G=
ENST00000695993.1:c.-104G=	ENSP00000512316.1:n.-104G=
ENST00000696006.1:c.-104G=	ENSP00000512325.1:n.-104G=
ENST00000696009.1:n.8G=
ENST00000696010.1:n.10G=
ENST00000696039.1:n.321+191G=
ENST00000696059.1:c.-104G=	ENSP00000512362.1:n.-104G=
ENST00000696060.1:c.-104G=	ENSP00000512363.1:n.-104G=
ENST00000696061.1:c.-104G=	ENSP00000512364.1:n.-104G=
ENST00000696062.1:c.96+389G=	ENSP00000512365.1:n.96+389G=
ENST00000696064.1:c.-118+191G=	ENSP00000512367.1:n.-118+191G=
ENST00000696065.1:c.-121+191G=	ENSP00000512368.1:n.-121+191G=
ENST00000696076.1:c.-104G=	ENSP00000512375.1:n.-104G=
ENST00000696077.1:c.-104G=	ENSP00000512376.1:n.-104G=
ENST00000696078.1:c.-104G=	ENSP00000512377.1:n.-104G=
ENST00000696080.1:c.-104G=	ENSP00000512379.1:n.-104G=
ENST00000372874.8:c.-104G=	ENSP00000361965.4:n.-104G=
ENST00000535573.1:n.332+191G=
ENST00000536076.1:n.213+191G=
NM_000022.2:c.-104G= , LRG_16t1:c.-104G=	NP_000013.2:n.-104G=
XM_011528479.1:c.-257+191G=	XP_011526781.1:n.-257+191G=
NM_000022.3:c.-104G=	NP_000013.2:n.-104G=
NM_001322050.1:c.-393G=	NP_001308979.1:n.-393G=
NM_001322051.1:c.-104G=	NP_001308980.1:n.-104G=
NR_136160.1:n.48G=