Canonical Allele Identifier: CA1515643529

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438803G= , CM000666.2:g.177438803G=	GRCh38
NC_000004.11:g.178359957G= , CM000666.1:g.178359957G=	GRCh37
NC_000004.10:g.178596951G=	NCBI36
NG_011845.2:g.8701C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.449C= MANE Select	ENSP00000264595.2:p.Ala150=
ENST00000264595.6:c.449C=	ENSP00000264595.2:p.Ala150=
ENST00000502310.5:c.104C=	ENSP00000423798.1:p.Ala35=
ENST00000506853.5:n.483C=
ENST00000510635.1:c.145C=
ENST00000510955.5:n.370C=
NM_000027.3:c.449C=	NP_000018.2:p.Ala150=
NM_001171988.1:c.449C=	NP_001165459.1:p.Ala150=
NR_033655.1:n.577C=
XM_006714123.2:c.449C=	XP_006714186.1:p.Ala150=
XR_001741155.2:n.543C=
NM_000027.4:c.449C= MANE Select	NP_000018.2:p.Ala150=
NM_001171988.2:c.449C=	NP_001165459.1:p.Ala150=
NR_033655.2:n.511C=