Canonical Allele Identifier: CA1515643383
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177438725T= , CM000666.2:g.177438725T= GRCh38
NC_000004.11:g.178359879T= , CM000666.1:g.178359879T= GRCh37
NC_000004.10:g.178596873T= NCBI36
NG_011845.2:g.8779A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.507+20A= MANE Select ENSP00000264595.2:n.507+20A=
ENST00000264595.6:c.507+20A= ENSP00000264595.2:n.507+20A=
ENST00000502310.5:c.162+20A= ENSP00000423798.1:n.162+20A=
ENST00000506853.5:n.541+20A=
ENST00000510635.1:c.203+20A=
ENST00000510955.5:n.428+20A=
NM_000027.3:c.507+20A= NP_000018.2:n.507+20A=
NM_001171988.1:c.507+20A= NP_001165459.1:n.507+20A=
NR_033655.1:n.635+20A=
XM_006714123.2:c.507+20A= XP_006714186.1:n.507+20A=
XR_001741155.2:n.601+20A=
NM_000027.4:c.507+20A= MANE Select NP_000018.2:n.507+20A=
NM_001171988.2:c.507+20A= NP_001165459.1:n.507+20A=
NR_033655.2:n.569+20A=