Canonical Allele Identifier: CA2014392192
Gene: C1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7086431T= , CM000674.2:g.7086431T= GRCh38
NG_062465.1:g.11177A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647956.2:c.1065A= MANE Select ENSP00000497341.1:p.Thr355=
ENST00000648162.1:n.1037A=
ENST00000649804.1:c.159A= ENSP00000497938.1:p.Thr53=
ENST00000535233.6:c.963A= ENSP00000438636.3:p.Thr321=
ENST00000536053.6:c.1107A= ENSP00000444271.3:p.Thr369=
ENST00000540394.5:n.2130A=
ENST00000542285.5:c.1065A= ENSP00000438615.2:p.Thr355=
ENST00000602298.2:n.1414A=
NM_001733.4:c.1065A= NP_001724.3:p.Thr355=
NM_001354346.1:c.1107A= NP_001341275.1:p.Thr369=
NM_001733.6:c.1065A= NP_001724.4:p.Thr355=
NM_001733.7:c.1065A= MANE Select NP_001724.4:p.Thr355=
NM_001354346.2:c.1107A= NP_001341275.1:p.Thr369=