Canonical Allele Identifier: CA1515643746
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177438894A= , CM000666.2:g.177438894A= GRCh38
NC_000004.11:g.178360048A= , CM000666.1:g.178360048A= GRCh37
NC_000004.10:g.178597042A= NCBI36
NG_011845.2:g.8610T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.395-37T= MANE Select ENSP00000264595.2:n.395-37T=
ENST00000264595.6:c.395-37T= ENSP00000264595.2:n.395-37T=
ENST00000502310.5:c.50-37T= ENSP00000423798.1:n.50-37T=
ENST00000506853.5:n.429-37T=
ENST00000510635.1:c.91-37T=
ENST00000510955.5:n.316-37T=
NM_000027.3:c.395-37T= NP_000018.2:n.395-37T=
NM_001171988.1:c.395-37T= NP_001165459.1:n.395-37T=
NR_033655.1:n.523-37T=
XM_006714123.2:c.395-37T= XP_006714186.1:n.395-37T=
XR_001741155.2:n.489-37T=
NM_000027.4:c.395-37T= MANE Select NP_000018.2:n.395-37T=
NM_001171988.2:c.395-37T= NP_001165459.1:n.395-37T=
NR_033655.2:n.457-37T=