Canonical Allele Identifier: CA691439027

Gene: C1R

Linked Data

• dbSNP Id: rs1232897873
• MyVariant Identifiers: chr12:g.7086496del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7086497del , CM000674.2:g.7086497del	GRCh38
NG_062465.1:g.11112del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647956.2:c.1039-39del MANE Select	ENSP00000497341.1:n.1039-39del
ENST00000648162.1:n.1011-39del
ENST00000649804.1:c.133-39del	ENSP00000497938.1:n.133-39del
ENST00000535233.6:c.937-39del	ENSP00000438636.3:n.937-39del
ENST00000536053.6:c.1081-39del	ENSP00000444271.3:n.1081-39del
ENST00000540394.5:n.2104-39del
ENST00000542285.5:c.1039-39del	ENSP00000438615.2:n.1039-39del
ENST00000602298.2:n.1349del
NM_001733.4:c.1039-39del	NP_001724.3:n.1039-39del
NM_001354346.1:c.1081-39del	NP_001341275.1:n.1081-39del
NM_001733.6:c.1039-39del	NP_001724.4:n.1039-39del
NM_001733.7:c.1039-39del MANE Select	NP_001724.4:n.1039-39del
NM_001354346.2:c.1081-39del	NP_001341275.1:n.1081-39del