Canonical Allele Identifier: CA2217060677

Gene: ARMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31462542G= , CM000678.2:g.31462542G=	GRCh38
NC_000016.9:g.31473863G= , CM000678.1:g.31473863G=	GRCh37
NC_000016.8:g.31381364G=	NCBI36
NG_034258.1:g.9270G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268314.9:c.995G= MANE Select	ENSP00000268314.4:p.Arg332=
ENST00000268314.8:c.995G=	ENSP00000268314.4:p.Arg332=
ENST00000408912.7:c.1280G=	ENSP00000386125.3:p.Arg427=
ENST00000457010.6:c.995G=	ENSP00000399561.2:p.Arg332=
ENST00000538189.5:c.503G=	ENSP00000443995.2:p.Arg168=
ENST00000563544.5:c.995G=	ENSP00000456877.1:p.Arg332=
ENST00000564900.1:c.213-230G=
NM_001105247.1:c.995G=	NP_001098717.1:p.Arg332=
NM_001288767.1:c.1280G=	NP_001275696.1:p.Arg427=
NM_001301820.1:c.1091G=	NP_001288749.1:p.Arg364=
NM_024742.2:c.995G=	NP_079018.1:p.Arg332=
XM_006721091.1:c.1091G=	XP_006721154.1:p.Arg364=
XM_006721091.3:c.1091G=	XP_006721154.1:p.Arg364=
XM_024450448.1:c.1091G=	XP_024306216.1:p.Arg364=
XM_024450449.1:c.1091G=	XP_024306217.1:p.Arg364=
NM_001105247.2:c.995G= MANE Select	NP_001098717.1:p.Arg332=
NM_001288767.2:c.1280G=	NP_001275696.1:p.Arg427=