Canonical Allele Identifier: CA1515643518

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438795C= , CM000666.2:g.177438795C=	GRCh38
NC_000004.11:g.178359949C= , CM000666.1:g.178359949C=	GRCh37
NC_000004.10:g.178596943C=	NCBI36
NG_011845.2:g.8709G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.457G= MANE Select	ENSP00000264595.2:p.Ala153=
ENST00000264595.6:c.457G=	ENSP00000264595.2:p.Ala153=
ENST00000502310.5:c.112G=	ENSP00000423798.1:p.Ala38=
ENST00000506853.5:n.491G=
ENST00000510635.1:c.153G=
ENST00000510955.5:n.378G=
NM_000027.3:c.457G=	NP_000018.2:p.Ala153=
NM_001171988.1:c.457G=	NP_001165459.1:p.Ala153=
NR_033655.1:n.585G=
XM_006714123.2:c.457G=	XP_006714186.1:p.Ala153=
XR_001741155.2:n.551G=
NM_000027.4:c.457G= MANE Select	NP_000018.2:p.Ala153=
NM_001171988.2:c.457G=	NP_001165459.1:p.Ala153=
NR_033655.2:n.519G=