Canonical Allele Identifier: CA1515641799

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437414C= , CM000666.2:g.177437414C=	GRCh38
NC_000004.11:g.178358568C= , CM000666.1:g.178358568C=	GRCh37
NC_000004.10:g.178595562C=	NCBI36
NG_011845.2:g.10090G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.613G= MANE Select	ENSP00000264595.2:p.Asp205=
ENST00000264595.6:c.613G=	ENSP00000264595.2:p.Asp205=
ENST00000502310.5:c.268G=	ENSP00000423798.1:p.Asp90=
ENST00000506853.5:n.647G=
ENST00000510635.1:c.309G=
ENST00000510955.5:n.534G=
NM_000027.3:c.613G=	NP_000018.2:p.Asp205=
NM_001171988.1:c.613G=	NP_001165459.1:p.Asp205=
NR_033655.1:n.741G=
XM_006714123.2:c.613G=	XP_006714186.1:p.Asp205=
XR_001741155.2:n.707G=
NM_000027.4:c.613G= MANE Select	NP_000018.2:p.Asp205=
NM_001171988.2:c.613G=	NP_001165459.1:p.Asp205=
NR_033655.2:n.675G=