Canonical Allele Identifier: CA2217060675
Gene: ARMC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31462536A= , CM000678.2:g.31462536A= GRCh38
NC_000016.9:g.31473857A= , CM000678.1:g.31473857A= GRCh37
NC_000016.8:g.31381358A= NCBI36
NG_034258.1:g.9264A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000268314.9:c.989A= MANE Select ENSP00000268314.4:p.Glu330=
ENST00000268314.8:c.989A= ENSP00000268314.4:p.Glu330=
ENST00000408912.7:c.1274A= ENSP00000386125.3:p.Glu425=
ENST00000457010.6:c.989A= ENSP00000399561.2:p.Glu330=
ENST00000538189.5:c.497A= ENSP00000443995.2:p.Glu166=
ENST00000563544.5:c.989A= ENSP00000456877.1:p.Glu330=
ENST00000564900.1:c.213-236A=
NM_001105247.1:c.989A= NP_001098717.1:p.Glu330=
NM_001288767.1:c.1274A= NP_001275696.1:p.Glu425=
NM_001301820.1:c.1085A= NP_001288749.1:p.Glu362=
NM_024742.2:c.989A= NP_079018.1:p.Glu330=
XM_006721091.1:c.1085A= XP_006721154.1:p.Glu362=
XM_006721091.3:c.1085A= XP_006721154.1:p.Glu362=
XM_024450448.1:c.1085A= XP_024306216.1:p.Glu362=
XM_024450449.1:c.1085A= XP_024306217.1:p.Glu362=
NM_001105247.2:c.989A= MANE Select NP_001098717.1:p.Glu330=
NM_001288767.2:c.1274A= NP_001275696.1:p.Glu425=