Canonical Allele Identifier: CA2617391416
Gene: C1R HGNC NCBI

Linked Data

gnomAD v4: 12-7086429-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7086429G>T , CM000674.2:g.7086429G>T GRCh38
NG_062465.1:g.11179C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647956.2:c.1067C>A MANE Select ENSP00000497341.1:p.Ala356Asp
ENST00000648162.1:n.1039C>A
ENST00000649804.1:c.161C>A ENSP00000497938.1:p.Ala54Asp
ENST00000535233.6:c.965C>A ENSP00000438636.3:p.Ala322Asp
ENST00000536053.6:c.1109C>A ENSP00000444271.3:p.Ala370Asp
ENST00000540394.5:n.2132C>A
ENST00000542285.5:c.1067C>A ENSP00000438615.2:p.Ala356Asp
ENST00000602298.2:n.1416C>A
NM_001733.4:c.1067C>A NP_001724.3:p.Ala356Asp
NM_001354346.1:c.1109C>A NP_001341275.1:p.Ala370Asp
NM_001733.6:c.1067C>A NP_001724.4:p.Ala356Asp
NM_001733.7:c.1067C>A MANE Select NP_001724.4:p.Ala356Asp
NM_001354346.2:c.1109C>A NP_001341275.1:p.Ala370Asp