Canonical Allele Identifier: CA494934138

Gene: ARMC5

Linked Data

• MyVariant Identifiers: chr16:g.31473972T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31462651T>G , CM000678.2:g.31462651T>G	GRCh38
NC_000016.9:g.31473972T>G , CM000678.1:g.31473972T>G	GRCh37
NC_000016.8:g.31381473T>G	NCBI36
NG_034258.1:g.9379T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268314.9:c.1104T>G MANE Select	ENSP00000268314.4:p.Ala368=
ENST00000268314.8:c.1104T>G	ENSP00000268314.4:p.Ala368=
ENST00000408912.7:c.1389T>G	ENSP00000386125.3:p.Ala463=
ENST00000457010.6:c.1104T>G	ENSP00000399561.2:p.Ala368=
ENST00000538189.5:c.612T>G	ENSP00000443995.2:p.Ala204=
ENST00000563544.5:c.1104T>G	ENSP00000456877.1:p.Ala368=
ENST00000564900.1:c.213-121T>G
NM_001105247.1:c.1104T>G	NP_001098717.1:p.Ala368=
NM_001288767.1:c.1389T>G	NP_001275696.1:p.Ala463=
NM_001301820.1:c.1200T>G	NP_001288749.1:p.Ala400=
NM_024742.2:c.1104T>G	NP_079018.1:p.Ala368=
XM_006721091.1:c.1200T>G	XP_006721154.1:p.Ala400=
XM_006721091.3:c.1200T>G	XP_006721154.1:p.Ala400=
XM_024450448.1:c.1200T>G	XP_024306216.1:p.Ala400=
XM_024450449.1:c.1200T>G	XP_024306217.1:p.Ala400=
NM_001105247.2:c.1104T>G MANE Select	NP_001098717.1:p.Ala368=
NM_001288767.2:c.1389T>G	NP_001275696.1:p.Ala463=