Canonical Allele Identifier: CA1515645788

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177440262G= , CM000666.2:g.177440262G=	GRCh38
NC_000004.11:g.178361416G= , CM000666.1:g.178361416G=	GRCh37
NC_000004.10:g.178598410G=	NCBI36
NG_011845.2:g.7242C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.281+11C= MANE Select	ENSP00000264595.2:n.281+11C=
ENST00000264595.6:c.281+11C=	ENSP00000264595.2:n.281+11C=
ENST00000506853.5:n.315+11C=
ENST00000510955.5:n.315+11C=
ENST00000511231.1:n.326C=
NM_000027.3:c.281+11C=	NP_000018.2:n.281+11C=
NM_001171988.1:c.281+11C=	NP_001165459.1:n.281+11C=
NR_033655.1:n.409+11C=
XM_006714123.2:c.281+11C=	XP_006714186.1:n.281+11C=
XR_001741155.2:n.375+11C=
NM_000027.4:c.281+11C= MANE Select	NP_000018.2:n.281+11C=
NM_001171988.2:c.281+11C=	NP_001165459.1:n.281+11C=
NR_033655.2:n.343+11C=