Canonical Allele Identifier: CA1515643399
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177438735G= , CM000666.2:g.177438735G= GRCh38
NC_000004.11:g.178359889G= , CM000666.1:g.178359889G= GRCh37
NC_000004.10:g.178596883G= NCBI36
NG_011845.2:g.8769C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.507+10C= MANE Select ENSP00000264595.2:n.507+10C=
ENST00000264595.6:c.507+10C= ENSP00000264595.2:n.507+10C=
ENST00000502310.5:c.162+10C= ENSP00000423798.1:n.162+10C=
ENST00000506853.5:n.541+10C=
ENST00000510635.1:c.203+10C=
ENST00000510955.5:n.428+10C=
NM_000027.3:c.507+10C= NP_000018.2:n.507+10C=
NM_001171988.1:c.507+10C= NP_001165459.1:n.507+10C=
NR_033655.1:n.635+10C=
XM_006714123.2:c.507+10C= XP_006714186.1:n.507+10C=
XR_001741155.2:n.601+10C=
NM_000027.4:c.507+10C= MANE Select NP_000018.2:n.507+10C=
NM_001171988.2:c.507+10C= NP_001165459.1:n.507+10C=
NR_033655.2:n.569+10C=