Canonical Allele Identifier: CA2587878440
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713658_6713659insGCCCAGCCCCCCACCTTGCCCCAC , CM000681.2:g.6713658_6713659insGCCCAGCCCCCCACCTTGCCCCAC GRCh38
NC_000019.9:g.6713669_6713670insGCCCAGCCCCCCACCTTGCCCCAC , CM000681.1:g.6713669_6713670insGCCCAGCCCCCCACCTTGCCCCAC GRCh37
NC_000019.8:g.6664669_6664670insGCCCAGCCCCCCACCTTGCCCCAC NCBI36
NG_009557.1:g.12000_12001insAAGGTGGGGGGCTGGGCGTGGGGC , LRG_27:g.12000_12001insAAGGTGGGGGGCTGGGCGTGGGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-143_651-142insAAGGTGGGGGGCTGGGCGTGGGGC ENSP00000512083.1:n.651-143_651-142insAAGGTGGGGGGCTGGGCGTGGGG...
ENST00000245907.11:c.774-143_774-142insAAGGTGGGGGGCTGGGCGTGGGGC MANE Select ENSP00000245907.4:n.774-143_774-142insAAGGTGGGGGGCTGGGCGTGGGG...
ENST00000245907.10:c.774-143_774-142insAAGGTGGGGGGCTGGGCGTGGGGC ENSP00000245907.4:n.774-143_774-142insAAGGTGGGGGGCTGGGCGTGGGG...
ENST00000595577.1:n.278-143_278-142insAAGGTGGGGGGCTGGGCGTGGGGC
ENST00000597442.5:n.23+114_23+115insAAGGTGGGGGGCTGGGCGTGGGGC
NM_000064.3:c.774-143_774-142insAAGGTGGGGGGCTGGGCGTGGGGC NP_000055.2:n.774-143_774-142insAAGGTGGGGGGCTGGGCGTGGGGC
NM_000064.4:c.774-143_774-142insAAGGTGGGGGGCTGGGCGTGGGGC MANE Select NP_000055.2:n.774-143_774-142insAAGGTGGGGGGCTGGGCGTGGGGC