Canonical Allele Identifier: CA1515637616
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177434425C= , CM000666.2:g.177434425C= GRCh38
NC_000004.11:g.178355579C= , CM000666.1:g.178355579C= GRCh37
NC_000004.10:g.178592573C= NCBI36
NG_011845.2:g.13079G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.763G= MANE Select ENSP00000264595.2:p.Ala255=
ENST00000264595.6:c.763G= ENSP00000264595.2:p.Ala255=
ENST00000502310.5:c.334G= ENSP00000423798.1:p.Ala112=
ENST00000506853.5:n.721G=
NM_000027.3:c.763G= NP_000018.2:p.Ala255=
NM_001171988.1:c.733G= NP_001165459.1:p.Ala245=
NR_033655.1:n.815G=
XM_006714123.2:c.*57G= XP_006714186.1:n.*57G=
XR_001741155.2:n.835G=
NM_000027.4:c.763G= MANE Select NP_000018.2:p.Ala255=
NM_001171988.2:c.733G= NP_001165459.1:p.Ala245=
NR_033655.2:n.749G=