Canonical Allele Identifier: CA1515643429

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438761T= , CM000666.2:g.177438761T=	GRCh38
NC_000004.11:g.178359915T= , CM000666.1:g.178359915T=	GRCh37
NC_000004.10:g.178596909T=	NCBI36
NG_011845.2:g.8743A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.491A= MANE Select	ENSP00000264595.2:p.Gln164=
ENST00000264595.6:c.491A=	ENSP00000264595.2:p.Gln164=
ENST00000502310.5:c.146A=	ENSP00000423798.1:p.Gln49=
ENST00000506853.5:n.525A=
ENST00000510635.1:c.187A=
ENST00000510955.5:n.412A=
NM_000027.3:c.491A=	NP_000018.2:p.Gln164=
NM_001171988.1:c.491A=	NP_001165459.1:p.Gln164=
NR_033655.1:n.619A=
XM_006714123.2:c.491A=	XP_006714186.1:p.Gln164=
XR_001741155.2:n.585A=
NM_000027.4:c.491A= MANE Select	NP_000018.2:p.Gln164=
NM_001171988.2:c.491A=	NP_001165459.1:p.Gln164=
NR_033655.2:n.553A=