Canonical Allele Identifier: CA1515649164
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442254T= , CM000666.2:g.177442254T= GRCh38
NC_000004.11:g.178363408T= , CM000666.1:g.178363408T= GRCh37
NC_000004.10:g.178600402T= NCBI36
NG_011845.2:g.5250A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.122A= MANE Select ENSP00000264595.2:p.Glu41=
ENST00000264595.6:c.122A= ENSP00000264595.2:p.Glu41=
ENST00000506853.5:n.156A=
ENST00000510955.5:n.156A=
ENST00000511231.1:n.156A=
NM_000027.3:c.122A= NP_000018.2:p.Glu41=
NM_001171988.1:c.122A= NP_001165459.1:p.Glu41=
NR_033655.1:n.250A=
XM_006714123.2:c.122A= XP_006714186.1:p.Glu41=
XR_001741155.2:n.216A=
NM_000027.4:c.122A= MANE Select NP_000018.2:p.Glu41=
NM_001171988.2:c.122A= NP_001165459.1:p.Glu41=
NR_033655.2:n.184A=