Canonical Allele Identifier: CA494934008

Gene: ARMC5

Linked Data

• gnomAD v4: 16-31462564-A-G
• MyVariant Identifiers: chr16:g.31473885A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31462564A>G , CM000678.2:g.31462564A>G	GRCh38
NC_000016.9:g.31473885A>G , CM000678.1:g.31473885A>G	GRCh37
NC_000016.8:g.31381386A>G	NCBI36
NG_034258.1:g.9292A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268314.9:c.1017A>G MANE Select	ENSP00000268314.4:p.Gly339=
ENST00000268314.8:c.1017A>G	ENSP00000268314.4:p.Gly339=
ENST00000408912.7:c.1302A>G	ENSP00000386125.3:p.Gly434=
ENST00000457010.6:c.1017A>G	ENSP00000399561.2:p.Gly339=
ENST00000538189.5:c.525A>G	ENSP00000443995.2:p.Gly175=
ENST00000563544.5:c.1017A>G	ENSP00000456877.1:p.Gly339=
ENST00000564900.1:c.213-208A>G
NM_001105247.1:c.1017A>G	NP_001098717.1:p.Gly339=
NM_001288767.1:c.1302A>G	NP_001275696.1:p.Gly434=
NM_001301820.1:c.1113A>G	NP_001288749.1:p.Gly371=
NM_024742.2:c.1017A>G	NP_079018.1:p.Gly339=
XM_006721091.1:c.1113A>G	XP_006721154.1:p.Gly371=
XM_006721091.3:c.1113A>G	XP_006721154.1:p.Gly371=
XM_024450448.1:c.1113A>G	XP_024306216.1:p.Gly371=
XM_024450449.1:c.1113A>G	XP_024306217.1:p.Gly371=
NM_001105247.2:c.1017A>G MANE Select	NP_001098717.1:p.Gly339=
NM_001288767.2:c.1302A>G	NP_001275696.1:p.Gly434=