Canonical Allele Identifier: CA494933886

Gene: ARMC5

Linked Data

• MyVariant Identifiers: chr16:g.31473843G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31462522G>A , CM000678.2:g.31462522G>A	GRCh38
NC_000016.9:g.31473843G>A , CM000678.1:g.31473843G>A	GRCh37
NC_000016.8:g.31381344G>A	NCBI36
NG_034258.1:g.9250G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268314.9:c.975G>A MANE Select	ENSP00000268314.4:p.Glu325=
ENST00000268314.8:c.975G>A	ENSP00000268314.4:p.Glu325=
ENST00000408912.7:c.1260G>A	ENSP00000386125.3:p.Glu420=
ENST00000457010.6:c.975G>A	ENSP00000399561.2:p.Glu325=
ENST00000538189.5:c.483G>A	ENSP00000443995.2:p.Glu161=
ENST00000563544.5:c.975G>A	ENSP00000456877.1:p.Glu325=
ENST00000564900.1:c.213-250G>A
NM_001105247.1:c.975G>A	NP_001098717.1:p.Glu325=
NM_001288767.1:c.1260G>A	NP_001275696.1:p.Glu420=
NM_001301820.1:c.1071G>A	NP_001288749.1:p.Glu357=
NM_024742.2:c.975G>A	NP_079018.1:p.Glu325=
XM_006721091.1:c.1071G>A	XP_006721154.1:p.Glu357=
XM_006721091.3:c.1071G>A	XP_006721154.1:p.Glu357=
XM_024450448.1:c.1071G>A	XP_024306216.1:p.Glu357=
XM_024450449.1:c.1071G>A	XP_024306217.1:p.Glu357=
NM_001105247.2:c.975G>A MANE Select	NP_001098717.1:p.Glu325=
NM_001288767.2:c.1260G>A	NP_001275696.1:p.Glu420=