Canonical Allele Identifier: CA1515641585

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437255C= , CM000666.2:g.177437255C=	GRCh38
NC_000004.11:g.178358409C= , CM000666.1:g.178358409C=	GRCh37
NC_000004.10:g.178595403C=	NCBI36
NG_011845.2:g.10249G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.622+150G= MANE Select	ENSP00000264595.2:n.622+150G=
ENST00000264595.6:c.622+150G=	ENSP00000264595.2:n.622+150G=
ENST00000502310.5:c.277+150G=	ENSP00000423798.1:n.277+150G=
ENST00000506853.5:n.656+150G=
ENST00000510635.1:c.318+150G=
ENST00000510955.5:n.693G=
NM_000027.3:c.622+150G=	NP_000018.2:n.622+150G=
NM_001171988.1:c.622+150G=	NP_001165459.1:n.622+150G=
NR_033655.1:n.750+150G=
XM_006714123.2:c.622+150G=	XP_006714186.1:n.622+150G=
XR_001741155.2:n.716+150G=
NM_000027.4:c.622+150G= MANE Select	NP_000018.2:n.622+150G=
NM_001171988.2:c.622+150G=	NP_001165459.1:n.622+150G=
NR_033655.2:n.684+150G=