Canonical Allele Identifier: CA1515641813

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437422C= , CM000666.2:g.177437422C=	GRCh38
NC_000004.11:g.178358576C= , CM000666.1:g.178358576C=	GRCh37
NC_000004.10:g.178595570C=	NCBI36
NG_011845.2:g.10082G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.605G= MANE Select	ENSP00000264595.2:p.Arg202=
ENST00000264595.6:c.605G=	ENSP00000264595.2:p.Arg202=
ENST00000502310.5:c.260G=	ENSP00000423798.1:p.Arg87=
ENST00000506853.5:n.639G=
ENST00000510635.1:c.301G=
ENST00000510955.5:n.526G=
NM_000027.3:c.605G=	NP_000018.2:p.Arg202=
NM_001171988.1:c.605G=	NP_001165459.1:p.Arg202=
NR_033655.1:n.733G=
XM_006714123.2:c.605G=	XP_006714186.1:p.Arg202=
XR_001741155.2:n.699G=
NM_000027.4:c.605G= MANE Select	NP_000018.2:p.Arg202=
NM_001171988.2:c.605G=	NP_001165459.1:p.Arg202=
NR_033655.2:n.667G=