Canonical Allele Identifier: CA1515643824
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177438941C= , CM000666.2:g.177438941C= GRCh38
NC_000004.11:g.178360095C= , CM000666.1:g.178360095C= GRCh37
NC_000004.10:g.178597089C= NCBI36
NG_011845.2:g.8563G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.395-84G= MANE Select ENSP00000264595.2:n.395-84G=
ENST00000264595.6:c.395-84G= ENSP00000264595.2:n.395-84G=
ENST00000502310.5:c.50-84G= ENSP00000423798.1:n.50-84G=
ENST00000506853.5:n.429-84G=
ENST00000510635.1:c.91-84G=
ENST00000510955.5:n.316-84G=
NM_000027.3:c.395-84G= NP_000018.2:n.395-84G=
NM_001171988.1:c.395-84G= NP_001165459.1:n.395-84G=
NR_033655.1:n.523-84G=
XM_006714123.2:c.395-84G= XP_006714186.1:n.395-84G=
XR_001741155.2:n.489-84G=
NM_000027.4:c.395-84G= MANE Select NP_000018.2:n.395-84G=
NM_001171988.2:c.395-84G= NP_001165459.1:n.395-84G=
NR_033655.2:n.457-84G=