Canonical Allele Identifier: CA2217060716

Gene: ARMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31462640C= , CM000678.2:g.31462640C=	GRCh38
NC_000016.9:g.31473961C= , CM000678.1:g.31473961C=	GRCh37
NC_000016.8:g.31381462C=	NCBI36
NG_034258.1:g.9368C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268314.9:c.1093C= MANE Select	ENSP00000268314.4:p.Leu365=
ENST00000268314.8:c.1093C=	ENSP00000268314.4:p.Leu365=
ENST00000408912.7:c.1378C=	ENSP00000386125.3:p.Leu460=
ENST00000457010.6:c.1093C=	ENSP00000399561.2:p.Leu365=
ENST00000538189.5:c.601C=	ENSP00000443995.2:p.Leu201=
ENST00000563544.5:c.1093C=	ENSP00000456877.1:p.Leu365=
ENST00000564900.1:c.213-132C=
NM_001105247.1:c.1093C=	NP_001098717.1:p.Leu365=
NM_001288767.1:c.1378C=	NP_001275696.1:p.Leu460=
NM_001301820.1:c.1189C=	NP_001288749.1:p.Leu397=
NM_024742.2:c.1093C=	NP_079018.1:p.Leu365=
XM_006721091.1:c.1189C=	XP_006721154.1:p.Leu397=
XM_006721091.3:c.1189C=	XP_006721154.1:p.Leu397=
XM_024450448.1:c.1189C=	XP_024306216.1:p.Leu397=
XM_024450449.1:c.1189C=	XP_024306217.1:p.Leu397=
NM_001105247.2:c.1093C= MANE Select	NP_001098717.1:p.Leu365=
NM_001288767.2:c.1378C=	NP_001275696.1:p.Leu460=