Canonical Allele Identifier: CA1515644050
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439101G= , CM000666.2:g.177439101G= GRCh38
NC_000004.11:g.178360255G= , CM000666.1:g.178360255G= GRCh37
NC_000004.10:g.178597249G= NCBI36
NG_011845.2:g.8403C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.395-244C= MANE Select ENSP00000264595.2:n.395-244C=
ENST00000264595.6:c.395-244C= ENSP00000264595.2:n.395-244C=
ENST00000502310.5:c.50-244C= ENSP00000423798.1:n.50-244C=
ENST00000506853.5:n.429-244C=
ENST00000510635.1:c.91-244C=
ENST00000510955.5:n.316-244C=
NM_000027.3:c.395-244C= NP_000018.2:n.395-244C=
NM_001171988.1:c.395-244C= NP_001165459.1:n.395-244C=
NR_033655.1:n.523-244C=
XM_006714123.2:c.395-244C= XP_006714186.1:n.395-244C=
XR_001741155.2:n.489-244C=
NM_000027.4:c.395-244C= MANE Select NP_000018.2:n.395-244C=
NM_001171988.2:c.395-244C= NP_001165459.1:n.395-244C=
NR_033655.2:n.457-244C=