Canonical Allele Identifier: CA1515649362

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177442315C= , CM000666.2:g.177442315C=	GRCh38
NC_000004.11:g.178363469C= , CM000666.1:g.178363469C=	GRCh37
NC_000004.10:g.178600463C=	NCBI36
NG_011845.2:g.5189G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.61G= MANE Select	ENSP00000264595.2:p.Val21=
ENST00000264595.6:c.61G=	ENSP00000264595.2:p.Val21=
ENST00000506853.5:n.95G=
ENST00000510955.5:n.95G=
ENST00000511231.1:n.95G=
NM_000027.3:c.61G=	NP_000018.2:p.Val21=
NM_001171988.1:c.61G=	NP_001165459.1:p.Val21=
NR_033655.1:n.189G=
XM_006714123.2:c.61G=	XP_006714186.1:p.Val21=
XR_001741155.2:n.155G=
NM_000027.4:c.61G= MANE Select	NP_000018.2:p.Val21=
NM_001171988.2:c.61G=	NP_001165459.1:p.Val21=
NR_033655.2:n.123G=