Canonical Allele Identifier: CA2014392171

Gene: C1R

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7086391G= , CM000674.2:g.7086391G=	GRCh38
NG_062465.1:g.11217C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647956.2:c.1105C= MANE Select	ENSP00000497341.1:p.Pro369=
ENST00000648162.1:n.1077C=
ENST00000649804.1:c.199C=	ENSP00000497938.1:p.Pro67=
ENST00000535233.6:c.1003C=	ENSP00000438636.3:p.Pro335=
ENST00000536053.6:c.1147C=	ENSP00000444271.3:p.Pro383=
ENST00000540394.5:n.2170C=
ENST00000542285.5:c.1105C=	ENSP00000438615.2:p.Pro369=
ENST00000602298.2:n.1454C=
NM_001733.4:c.1105C=	NP_001724.3:p.Pro369=
NM_001354346.1:c.1147C=	NP_001341275.1:p.Pro383=
NM_001733.6:c.1105C=	NP_001724.4:p.Pro369=
NM_001733.7:c.1105C= MANE Select	NP_001724.4:p.Pro369=
NM_001354346.2:c.1147C=	NP_001341275.1:p.Pro383=