Canonical Allele Identifier: CA1515641759

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437388C= , CM000666.2:g.177437388C=	GRCh38
NC_000004.11:g.178358542C= , CM000666.1:g.178358542C=	GRCh37
NC_000004.10:g.178595536C=	NCBI36
NG_011845.2:g.10116G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.622+17G= MANE Select	ENSP00000264595.2:n.622+17G=
ENST00000264595.6:c.622+17G=	ENSP00000264595.2:n.622+17G=
ENST00000502310.5:c.277+17G=	ENSP00000423798.1:n.277+17G=
ENST00000506853.5:n.656+17G=
ENST00000510635.1:c.318+17G=
ENST00000510955.5:n.560G=
NM_000027.3:c.622+17G=	NP_000018.2:n.622+17G=
NM_001171988.1:c.622+17G=	NP_001165459.1:n.622+17G=
NR_033655.1:n.750+17G=
XM_006714123.2:c.622+17G=	XP_006714186.1:n.622+17G=
XR_001741155.2:n.716+17G=
NM_000027.4:c.622+17G= MANE Select	NP_000018.2:n.622+17G=
NM_001171988.2:c.622+17G=	NP_001165459.1:n.622+17G=
NR_033655.2:n.684+17G=