Canonical Allele Identifier: CA1515644500
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439509G= , CM000666.2:g.177439509G= GRCh38
NC_000004.11:g.178360663G= , CM000666.1:g.178360663G= GRCh37
NC_000004.10:g.178597657G= NCBI36
NG_011845.2:g.7995C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.394+67C= MANE Select ENSP00000264595.2:n.394+67C=
ENST00000264595.6:c.394+67C= ENSP00000264595.2:n.394+67C=
ENST00000502310.5:c.49+67C= ENSP00000423798.1:n.49+67C=
ENST00000506853.5:n.428+67C=
ENST00000510635.1:c.90+67C=
ENST00000510955.5:n.316-652C=
NM_000027.3:c.394+67C= NP_000018.2:n.394+67C=
NM_001171988.1:c.394+67C= NP_001165459.1:n.394+67C=
NR_033655.1:n.522+67C=
XM_006714123.2:c.394+67C= XP_006714186.1:n.394+67C=
XR_001741155.2:n.488+67C=
NM_000027.4:c.394+67C= MANE Select NP_000018.2:n.394+67C=
NM_001171988.2:c.394+67C= NP_001165459.1:n.394+67C=
NR_033655.2:n.456+67C=