Canonical Allele Identifier: CA1515643421

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438749C= , CM000666.2:g.177438749C=	GRCh38
NC_000004.11:g.178359903C= , CM000666.1:g.178359903C=	GRCh37
NC_000004.10:g.178596897C=	NCBI36
NG_011845.2:g.8755G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.503G= MANE Select	ENSP00000264595.2:p.Trp168=
ENST00000264595.6:c.503G=	ENSP00000264595.2:p.Trp168=
ENST00000502310.5:c.158G=	ENSP00000423798.1:p.Trp53=
ENST00000506853.5:n.537G=
ENST00000510635.1:c.199G=
ENST00000510955.5:n.424G=
NM_000027.3:c.503G=	NP_000018.2:p.Trp168=
NM_001171988.1:c.503G=	NP_001165459.1:p.Trp168=
NR_033655.1:n.631G=
XM_006714123.2:c.503G=	XP_006714186.1:p.Trp168=
XR_001741155.2:n.597G=
NM_000027.4:c.503G= MANE Select	NP_000018.2:p.Trp168=
NM_001171988.2:c.503G=	NP_001165459.1:p.Trp168=
NR_033655.2:n.565G=