Canonical Allele Identifier: CA2617391443

Gene: C1R

Linked Data

• gnomAD v4: 12-7086479-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7086479T>G , CM000674.2:g.7086479T>G	GRCh38
NG_062465.1:g.11129A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647956.2:c.1039-22A>C MANE Select	ENSP00000497341.1:n.1039-22A>C
ENST00000648162.1:n.1011-22A>C
ENST00000649804.1:c.133-22A>C	ENSP00000497938.1:n.133-22A>C
ENST00000535233.6:c.937-22A>C	ENSP00000438636.3:n.937-22A>C
ENST00000536053.6:c.1081-22A>C	ENSP00000444271.3:n.1081-22A>C
ENST00000540394.5:n.2104-22A>C
ENST00000542285.5:c.1039-22A>C	ENSP00000438615.2:n.1039-22A>C
ENST00000602298.2:n.1366A>C
NM_001733.4:c.1039-22A>C	NP_001724.3:n.1039-22A>C
NM_001354346.1:c.1081-22A>C	NP_001341275.1:n.1081-22A>C
NM_001733.6:c.1039-22A>C	NP_001724.4:n.1039-22A>C
NM_001733.7:c.1039-22A>C MANE Select	NP_001724.4:n.1039-22A>C
NM_001354346.2:c.1081-22A>C	NP_001341275.1:n.1081-22A>C