Canonical Allele Identifier: CA2732051727
Gene: ARMC5 HGNC NCBI

Linked Data

dbSNP Id: rs2142569163

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31462541del , CM000678.2:g.31462541del GRCh38
NC_000016.9:g.31473862del , CM000678.1:g.31473862del GRCh37
NC_000016.8:g.31381363del NCBI36
NG_034258.1:g.9269del

Transcript Alleles

HGVS Amino-acid Change
ENST00000268314.9:c.994del MANE Select ENSP00000268314.4:p.Arg332GlyfsTer?
ENST00000268314.8:c.994del ENSP00000268314.4:p.Arg332GlyfsTer?
ENST00000408912.7:c.1279del ENSP00000386125.3:p.Arg427GlyfsTer?
ENST00000457010.6:c.994del ENSP00000399561.2:p.Arg332GlyfsTer?
ENST00000538189.5:c.502del ENSP00000443995.2:p.Arg168GlyfsTer?
ENST00000563544.5:c.994del ENSP00000456877.1:p.Arg332GlyfsTer?
ENST00000564900.1:c.213-231del
NM_001105247.1:c.994del NP_001098717.1:p.Arg332GlyfsTer?
NM_001288767.1:c.1279del NP_001275696.1:p.Arg427GlyfsTer?
NM_001301820.1:c.1090del NP_001288749.1:p.Arg364GlyfsTer?
NM_024742.2:c.994del NP_079018.1:p.Arg332GlyfsTer?
XM_006721091.1:c.1090del XP_006721154.1:p.Arg364GlyfsTer?
XM_006721091.3:c.1090del XP_006721154.1:p.Arg364GlyfsTer?
XM_024450448.1:c.1090del XP_024306216.1:p.Arg364GlyfsTer?
XM_024450449.1:c.1090del XP_024306217.1:p.Arg364GlyfsTer?
NM_001105247.2:c.994del MANE Select NP_001098717.1:p.Arg332GlyfsTer?
NM_001288767.2:c.1279del NP_001275696.1:p.Arg427GlyfsTer?