Canonical Allele Identifier: CA2794437761

Gene: C1R

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7086589_7086599del , CM000674.2:g.7086589_7086599del	GRCh38
NG_062465.1:g.11009_11019del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647956.2:c.1039-142_1039-132del MANE Select	ENSP00000497341.1:n.1039-142_1039-132del
ENST00000648162.1:n.1011-142_1011-132del
ENST00000649804.1:c.133-142_133-132del	ENSP00000497938.1:n.133-142_133-132del
ENST00000535233.6:c.937-142_937-132del	ENSP00000438636.3:n.937-142_937-132del
ENST00000536053.6:c.1081-142_1081-132del	ENSP00000444271.3:n.1081-142_1081-132del
ENST00000540394.5:n.2104-142_2104-132del
ENST00000542285.5:c.1039-142_1039-132del	ENSP00000438615.2:n.1039-142_1039-132del
ENST00000602298.2:n.1246_1256del
NM_001733.4:c.1039-142_1039-132del	NP_001724.3:n.1039-142_1039-132del
NM_001354346.1:c.1081-142_1081-132del	NP_001341275.1:n.1081-142_1081-132del
NM_001733.6:c.1039-142_1039-132del	NP_001724.4:n.1039-142_1039-132del
NM_001733.7:c.1039-142_1039-132del MANE Select	NP_001724.4:n.1039-142_1039-132del
NM_001354346.2:c.1081-142_1081-132del	NP_001341275.1:n.1081-142_1081-132del