Canonical Allele Identifier: CA1515637898

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177434578T= , CM000666.2:g.177434578T=	GRCh38
NC_000004.11:g.178355732T= , CM000666.1:g.178355732T=	GRCh37
NC_000004.10:g.178592726T=	NCBI36
NG_011845.2:g.12926A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.699-89A= MANE Select	ENSP00000264595.2:n.699-89A=
ENST00000264595.6:c.699-89A=	ENSP00000264595.2:n.699-89A=
ENST00000502310.5:c.278-97A=	ENSP00000423798.1:n.278-97A=
ENST00000506853.5:n.657-89A=
ENST00000510635.1:c.373-97A=
NM_000027.3:c.699-89A=	NP_000018.2:n.699-89A=
NM_001171988.1:c.677-97A=	NP_001165459.1:n.677-97A=
NR_033655.1:n.751-89A=
XM_006714123.2:c.677-89A=	XP_006714186.1:n.677-89A=
XR_001741155.2:n.771-89A=
NM_000027.4:c.699-89A= MANE Select	NP_000018.2:n.699-89A=
NM_001171988.2:c.677-97A=	NP_001165459.1:n.677-97A=
NR_033655.2:n.685-89A=