Canonical Allele Identifier: CA494933875

Gene: ARMC5

Linked Data

• MyVariant Identifiers: chr16:g.31473840G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31462519G>A , CM000678.2:g.31462519G>A	GRCh38
NC_000016.9:g.31473840G>A , CM000678.1:g.31473840G>A	GRCh37
NC_000016.8:g.31381341G>A	NCBI36
NG_034258.1:g.9247G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268314.9:c.972G>A MANE Select	ENSP00000268314.4:p.Val324=
ENST00000268314.8:c.972G>A	ENSP00000268314.4:p.Val324=
ENST00000408912.7:c.1257G>A	ENSP00000386125.3:p.Val419=
ENST00000457010.6:c.972G>A	ENSP00000399561.2:p.Val324=
ENST00000538189.5:c.480G>A	ENSP00000443995.2:p.Val160=
ENST00000563544.5:c.972G>A	ENSP00000456877.1:p.Val324=
ENST00000564900.1:c.213-253G>A
NM_001105247.1:c.972G>A	NP_001098717.1:p.Val324=
NM_001288767.1:c.1257G>A	NP_001275696.1:p.Val419=
NM_001301820.1:c.1068G>A	NP_001288749.1:p.Val356=
NM_024742.2:c.972G>A	NP_079018.1:p.Val324=
XM_006721091.1:c.1068G>A	XP_006721154.1:p.Val356=
XM_006721091.3:c.1068G>A	XP_006721154.1:p.Val356=
XM_024450448.1:c.1068G>A	XP_024306216.1:p.Val356=
XM_024450449.1:c.1068G>A	XP_024306217.1:p.Val356=
NM_001105247.2:c.972G>A MANE Select	NP_001098717.1:p.Val324=
NM_001288767.2:c.1257G>A	NP_001275696.1:p.Val419=