Canonical Allele Identifier: CA2014392084

Gene: C1R

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7086170T= , CM000674.2:g.7086170T=	GRCh38
NG_062465.1:g.11438A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647956.2:c.1118-154A= MANE Select	ENSP00000497341.1:n.1118-154A=
ENST00000648162.1:n.1090-154A=
ENST00000649804.1:c.211+209A=	ENSP00000497938.1:n.211+209A=
ENST00000535233.6:c.1016-154A=	ENSP00000438636.3:n.1016-154A=
ENST00000536053.6:c.1160-154A=	ENSP00000444271.3:n.1160-154A=
ENST00000540394.5:n.2183-154A=
ENST00000542285.5:c.1118-154A=	ENSP00000438615.2:n.1118-154A=
ENST00000602298.2:n.1467-154A=
NM_001733.4:c.1118-154A=	NP_001724.3:n.1118-154A=
NM_001354346.1:c.1160-154A=	NP_001341275.1:n.1160-154A=
NM_001733.6:c.1118-154A=	NP_001724.4:n.1118-154A=
NM_001733.7:c.1118-154A= MANE Select	NP_001724.4:n.1118-154A=
NM_001354346.2:c.1160-154A=	NP_001341275.1:n.1160-154A=