Canonical Allele Identifier: CA2617391381

Gene: C1R

Linked Data

• dbSNP Id: rs2135741308
• gnomAD v4: 12-7086382-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7086382T>G , CM000674.2:g.7086382T>G	GRCh38
NG_062465.1:g.11226A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647956.2:c.1114A>C MANE Select	ENSP00000497341.1:p.Lys372Gln
ENST00000648162.1:n.1086A>C
ENST00000649804.1:c.208A>C	ENSP00000497938.1:p.Lys70Gln
ENST00000535233.6:c.1012A>C	ENSP00000438636.3:p.Lys338Gln
ENST00000536053.6:c.1156A>C	ENSP00000444271.3:p.Lys386Gln
ENST00000540394.5:n.2179A>C
ENST00000542285.5:c.1114A>C	ENSP00000438615.2:p.Lys372Gln
ENST00000602298.2:n.1463A>C
NM_001733.4:c.1114A>C	NP_001724.3:p.Lys372Gln
NM_001354346.1:c.1156A>C	NP_001341275.1:p.Lys386Gln
NM_001733.6:c.1114A>C	NP_001724.4:p.Lys372Gln
NM_001733.7:c.1114A>C MANE Select	NP_001724.4:p.Lys372Gln
NM_001354346.2:c.1156A>C	NP_001341275.1:p.Lys386Gln