Canonical Allele Identifier: CA1515637857

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177434526G= , CM000666.2:g.177434526G=	GRCh38
NC_000004.11:g.178355680G= , CM000666.1:g.178355680G=	GRCh37
NC_000004.10:g.178592674G=	NCBI36
NG_011845.2:g.12978C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.699-37C= MANE Select	ENSP00000264595.2:n.699-37C=
ENST00000264595.6:c.699-37C=	ENSP00000264595.2:n.699-37C=
ENST00000502310.5:c.278-45C=	ENSP00000423798.1:n.278-45C=
ENST00000506853.5:n.657-37C=
ENST00000510635.1:c.373-45C=
NM_000027.3:c.699-37C=	NP_000018.2:n.699-37C=
NM_001171988.1:c.677-45C=	NP_001165459.1:n.677-45C=
NR_033655.1:n.751-37C=
XM_006714123.2:c.677-37C=	XP_006714186.1:n.677-37C=
XR_001741155.2:n.771-37C=
NM_000027.4:c.699-37C= MANE Select	NP_000018.2:n.699-37C=
NM_001171988.2:c.677-45C=	NP_001165459.1:n.677-45C=
NR_033655.2:n.685-37C=