Canonical Allele Identifier: CA2217060720

Gene: ARMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31462649G= , CM000678.2:g.31462649G=	GRCh38
NC_000016.9:g.31473970G= , CM000678.1:g.31473970G=	GRCh37
NC_000016.8:g.31381471G=	NCBI36
NG_034258.1:g.9377G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268314.9:c.1102G= MANE Select	ENSP00000268314.4:p.Ala368=
ENST00000268314.8:c.1102G=	ENSP00000268314.4:p.Ala368=
ENST00000408912.7:c.1387G=	ENSP00000386125.3:p.Ala463=
ENST00000457010.6:c.1102G=	ENSP00000399561.2:p.Ala368=
ENST00000538189.5:c.610G=	ENSP00000443995.2:p.Ala204=
ENST00000563544.5:c.1102G=	ENSP00000456877.1:p.Ala368=
ENST00000564900.1:c.213-123G=
NM_001105247.1:c.1102G=	NP_001098717.1:p.Ala368=
NM_001288767.1:c.1387G=	NP_001275696.1:p.Ala463=
NM_001301820.1:c.1198G=	NP_001288749.1:p.Ala400=
NM_024742.2:c.1102G=	NP_079018.1:p.Ala368=
XM_006721091.1:c.1198G=	XP_006721154.1:p.Ala400=
XM_006721091.3:c.1198G=	XP_006721154.1:p.Ala400=
XM_024450448.1:c.1198G=	XP_024306216.1:p.Ala400=
XM_024450449.1:c.1198G=	XP_024306217.1:p.Ala400=
NM_001105247.2:c.1102G= MANE Select	NP_001098717.1:p.Ala368=
NM_001288767.2:c.1387G=	NP_001275696.1:p.Ala463=