Canonical Allele Identifier: CA2587876975
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709611_6709612insGGGCCCCCCC , CM000681.2:g.6709611_6709612insGGGCCCCCCC GRCh38
NC_000019.9:g.6709622_6709623insGGGCCCCCCC , CM000681.1:g.6709622_6709623insGGGCCCCCCC GRCh37
NC_000019.8:g.6660622_6660623insGGGCCCCCCC NCBI36
NG_009557.1:g.16040_16041insGGGGGGGCCC , LRG_27:g.16040_16041insGGGGGGGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1722+72_1722+73insGGGGGGGCCC ENSP00000512083.1:n.1722+72_1722+73insGGGGGGGCCC
ENST00000695654.1:c.969+72_969+73insGGGGGGGCCC ENSP00000512085.1:n.969+72_969+73insGGGGGGGCCC
ENST00000695655.1:c.786+72_786+73insGGGGGGGCCC ENSP00000512086.1:n.786+72_786+73insGGGGGGGCCC
ENST00000695692.1:n.1209+72_1209+73insGGGGGGGCCC
ENST00000245907.11:c.1845+72_1845+73insGGGGGGGCCC MANE Select ENSP00000245907.4:n.1845+72_1845+73insGGGGGGGCCC
ENST00000245907.10:c.1845+72_1845+73insGGGGGGGCCC ENSP00000245907.4:n.1845+72_1845+73insGGGGGGGCCC
NM_000064.3:c.1845+72_1845+73insGGGGGGGCCC NP_000055.2:n.1845+72_1845+73insGGGGGGGCCC
NM_000064.4:c.1845+72_1845+73insGGGGGGGCCC MANE Select NP_000055.2:n.1845+72_1845+73insGGGGGGGCCC