Canonical Allele Identifier: CA2014392200
Gene: C1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7086452G= , CM000674.2:g.7086452G= GRCh38
NG_062465.1:g.11156C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647956.2:c.1044C= MANE Select ENSP00000497341.1:p.Asn348=
ENST00000648162.1:n.1016C=
ENST00000649804.1:c.138C= ENSP00000497938.1:p.Asn46=
ENST00000535233.6:c.942C= ENSP00000438636.3:p.Asn314=
ENST00000536053.6:c.1086C= ENSP00000444271.3:p.Asn362=
ENST00000540394.5:n.2109C=
ENST00000542285.5:c.1044C= ENSP00000438615.2:p.Asn348=
ENST00000602298.2:n.1393C=
NM_001733.4:c.1044C= NP_001724.3:p.Asn348=
NM_001354346.1:c.1086C= NP_001341275.1:p.Asn362=
NM_001733.6:c.1044C= NP_001724.4:p.Asn348=
NM_001733.7:c.1044C= MANE Select NP_001724.4:p.Asn348=
NM_001354346.2:c.1086C= NP_001341275.1:p.Asn362=