Canonical Allele Identifier: CA2320568056
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713664_6713665delinsGC , CM000681.2:g.6713664_6713665delinsGC GRCh38
NC_000019.9:g.6713675_6713676delinsGC , CM000681.1:g.6713675_6713676delinsGC GRCh37
NC_000019.8:g.6664675_6664676delinsGC NCBI36
NG_009557.1:g.11987_11988delinsGC , LRG_27:g.11987_11988delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-156_651-155delinsGC ENSP00000512083.1:n.651-156_651-155delinsGC
ENST00000245907.11:c.774-156_774-155delinsGC MANE Select ENSP00000245907.4:n.774-156_774-155delinsGC
ENST00000245907.10:c.774-156_774-155delinsGC ENSP00000245907.4:n.774-156_774-155delinsGC
ENST00000595577.1:n.278-156_278-155delinsGC
ENST00000597442.5:n.23+101_23+102delinsGC
NM_000064.3:c.774-156_774-155delinsGC NP_000055.2:n.774-156_774-155delinsGC
NM_000064.4:c.774-156_774-155delinsGC MANE Select NP_000055.2:n.774-156_774-155delinsGC