Canonical Allele Identifier: CA2014392207
Gene: C1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7086468G= , CM000674.2:g.7086468G= GRCh38
NG_062465.1:g.11140C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647956.2:c.1039-11C= MANE Select ENSP00000497341.1:n.1039-11C=
ENST00000648162.1:n.1011-11C=
ENST00000649804.1:c.133-11C= ENSP00000497938.1:n.133-11C=
ENST00000535233.6:c.937-11C= ENSP00000438636.3:n.937-11C=
ENST00000536053.6:c.1081-11C= ENSP00000444271.3:n.1081-11C=
ENST00000540394.5:n.2104-11C=
ENST00000542285.5:c.1039-11C= ENSP00000438615.2:n.1039-11C=
ENST00000602298.2:n.1377C=
NM_001733.4:c.1039-11C= NP_001724.3:n.1039-11C=
NM_001354346.1:c.1081-11C= NP_001341275.1:n.1081-11C=
NM_001733.6:c.1039-11C= NP_001724.4:n.1039-11C=
NM_001733.7:c.1039-11C= MANE Select NP_001724.4:n.1039-11C=
NM_001354346.2:c.1081-11C= NP_001341275.1:n.1081-11C=