Canonical Allele Identifier: CA1515637766

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177434488G= , CM000666.2:g.177434488G=	GRCh38
NC_000004.11:g.178355642G= , CM000666.1:g.178355642G=	GRCh37
NC_000004.10:g.178592636G=	NCBI36
NG_011845.2:g.13016C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.700C= MANE Select	ENSP00000264595.2:p.Arg234=
ENST00000264595.6:c.700C=	ENSP00000264595.2:p.Arg234=
ENST00000502310.5:c.278-7C=	ENSP00000423798.1:n.278-7C=
ENST00000506853.5:n.658C=
ENST00000510635.1:c.373-7C=
NM_000027.3:c.700C=	NP_000018.2:p.Arg234=
NM_001171988.1:c.677-7C=	NP_001165459.1:n.677-7C=
NR_033655.1:n.752C=
XM_006714123.2:c.678C=	XP_006714186.1:p.Ala226=
XR_001741155.2:n.772C=
NM_000027.4:c.700C= MANE Select	NP_000018.2:p.Arg234=
NM_001171988.2:c.677-7C=	NP_001165459.1:n.677-7C=
NR_033655.2:n.686C=