Canonical Allele Identifier: CA2014392169

Gene: C1R

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7086387C= , CM000674.2:g.7086387C=	GRCh38
NG_062465.1:g.11221G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647956.2:c.1109G= MANE Select	ENSP00000497341.1:p.Arg370=
ENST00000648162.1:n.1081G=
ENST00000649804.1:c.203G=	ENSP00000497938.1:p.Arg68=
ENST00000535233.6:c.1007G=	ENSP00000438636.3:p.Arg336=
ENST00000536053.6:c.1151G=	ENSP00000444271.3:p.Arg384=
ENST00000540394.5:n.2174G=
ENST00000542285.5:c.1109G=	ENSP00000438615.2:p.Arg370=
ENST00000602298.2:n.1458G=
NM_001733.4:c.1109G=	NP_001724.3:p.Arg370=
NM_001354346.1:c.1151G=	NP_001341275.1:p.Arg384=
NM_001733.6:c.1109G=	NP_001724.4:p.Arg370=
NM_001733.7:c.1109G= MANE Select	NP_001724.4:p.Arg370=
NM_001354346.2:c.1151G=	NP_001341275.1:p.Arg384=