Canonical Allele Identifier: CA2014392191

Gene: C1R

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7086429G= , CM000674.2:g.7086429G=	GRCh38
NG_062465.1:g.11179C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647956.2:c.1067C= MANE Select	ENSP00000497341.1:p.Ala356=
ENST00000648162.1:n.1039C=
ENST00000649804.1:c.161C=	ENSP00000497938.1:p.Ala54=
ENST00000535233.6:c.965C=	ENSP00000438636.3:p.Ala322=
ENST00000536053.6:c.1109C=	ENSP00000444271.3:p.Ala370=
ENST00000540394.5:n.2132C=
ENST00000542285.5:c.1067C=	ENSP00000438615.2:p.Ala356=
ENST00000602298.2:n.1416C=
NM_001733.4:c.1067C=	NP_001724.3:p.Ala356=
NM_001354346.1:c.1109C=	NP_001341275.1:p.Ala370=
NM_001733.6:c.1067C=	NP_001724.4:p.Ala356=
NM_001733.7:c.1067C= MANE Select	NP_001724.4:p.Ala356=
NM_001354346.2:c.1109C=	NP_001341275.1:p.Ala370=