Canonical Allele Identifier: CA1515637622
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177434426G= , CM000666.2:g.177434426G= GRCh38
NC_000004.11:g.178355580G= , CM000666.1:g.178355580G= GRCh37
NC_000004.10:g.178592574G= NCBI36
NG_011845.2:g.13078C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.762C= MANE Select ENSP00000264595.2:p.Ala254=
ENST00000264595.6:c.762C= ENSP00000264595.2:p.Ala254=
ENST00000502310.5:c.333C= ENSP00000423798.1:p.Ala111=
ENST00000506853.5:n.720C=
NM_000027.3:c.762C= NP_000018.2:p.Ala254=
NM_001171988.1:c.732C= NP_001165459.1:p.Ala244=
NR_033655.1:n.814C=
XM_006714123.2:c.*56C= XP_006714186.1:n.*56C=
XR_001741155.2:n.834C=
NM_000027.4:c.762C= MANE Select NP_000018.2:p.Ala254=
NM_001171988.2:c.732C= NP_001165459.1:p.Ala244=
NR_033655.2:n.748C=