Canonical Allele Identifier: CA2014392145
Gene: C1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7086327C= , CM000674.2:g.7086327C= GRCh38
NG_062465.1:g.11281G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647956.2:c.1117+52G= MANE Select ENSP00000497341.1:n.1117+52G=
ENST00000648162.1:n.1089+52G=
ENST00000649804.1:c.211+52G= ENSP00000497938.1:n.211+52G=
ENST00000535233.6:c.1015+52G= ENSP00000438636.3:n.1015+52G=
ENST00000536053.6:c.1159+52G= ENSP00000444271.3:n.1159+52G=
ENST00000540394.5:n.2182+52G=
ENST00000542285.5:c.1117+52G= ENSP00000438615.2:n.1117+52G=
ENST00000602298.2:n.1466+52G=
NM_001733.4:c.1117+52G= NP_001724.3:n.1117+52G=
NM_001354346.1:c.1159+52G= NP_001341275.1:n.1159+52G=
NM_001733.6:c.1117+52G= NP_001724.4:n.1117+52G=
NM_001733.7:c.1117+52G= MANE Select NP_001724.4:n.1117+52G=
NM_001354346.2:c.1159+52G= NP_001341275.1:n.1159+52G=