Canonical Allele Identifier: CA1515649642

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177442369G= , CM000666.2:g.177442369G=	GRCh38
NC_000004.11:g.178363523G= , CM000666.1:g.178363523G=	GRCh37
NC_000004.10:g.178600517G=	NCBI36
NG_011845.2:g.5135C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.7C= MANE Select	ENSP00000264595.2:p.Arg3=
ENST00000264595.6:c.7C=	ENSP00000264595.2:p.Arg3=
ENST00000506853.5:n.41C=
ENST00000510955.5:n.41C=
ENST00000511231.1:n.41C=
NM_000027.3:c.7C=	NP_000018.2:p.Arg3=
NM_001171988.1:c.7C=	NP_001165459.1:p.Arg3=
NR_033655.1:n.135C=
XM_006714123.2:c.7C=	XP_006714186.1:p.Arg3=
XR_001741155.2:n.101C=
NM_000027.4:c.7C= MANE Select	NP_000018.2:p.Arg3=
NM_001171988.2:c.7C=	NP_001165459.1:p.Arg3=
NR_033655.2:n.69C=