Canonical Allele Identifier: CA1515643478

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438774C= , CM000666.2:g.177438774C=	GRCh38
NC_000004.11:g.178359928C= , CM000666.1:g.178359928C=	GRCh37
NC_000004.10:g.178596922C=	NCBI36
NG_011845.2:g.8730G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.478G= MANE Select	ENSP00000264595.2:p.Ala160=
ENST00000264595.6:c.478G=	ENSP00000264595.2:p.Ala160=
ENST00000502310.5:c.133G=	ENSP00000423798.1:p.Ala45=
ENST00000506853.5:n.512G=
ENST00000510635.1:c.174G=
ENST00000510955.5:n.399G=
NM_000027.3:c.478G=	NP_000018.2:p.Ala160=
NM_001171988.1:c.478G=	NP_001165459.1:p.Ala160=
NR_033655.1:n.606G=
XM_006714123.2:c.478G=	XP_006714186.1:p.Ala160=
XR_001741155.2:n.572G=
NM_000027.4:c.478G= MANE Select	NP_000018.2:p.Ala160=
NM_001171988.2:c.478G=	NP_001165459.1:p.Ala160=
NR_033655.2:n.540G=