Canonical Allele Identifier: CA2587877261
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709618_6709619insCCCACCCCC , CM000681.2:g.6709618_6709619insCCCACCCCC GRCh38
NC_000019.9:g.6709629_6709630insCCCACCCCC , CM000681.1:g.6709629_6709630insCCCACCCCC GRCh37
NC_000019.8:g.6660629_6660630insCCCACCCCC NCBI36
NG_009557.1:g.16036_16037insGGTGGGGGG , LRG_27:g.16036_16037insGGTGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1722+68_1722+69insGGTGGGGGG ENSP00000512083.1:n.1722+68_1722+69insGGTGGGGGG
ENST00000695654.1:c.969+68_969+69insGGTGGGGGG ENSP00000512085.1:n.969+68_969+69insGGTGGGGGG
ENST00000695655.1:c.786+68_786+69insGGTGGGGGG ENSP00000512086.1:n.786+68_786+69insGGTGGGGGG
ENST00000695692.1:n.1209+68_1209+69insGGTGGGGGG
ENST00000245907.11:c.1845+68_1845+69insGGTGGGGGG MANE Select ENSP00000245907.4:n.1845+68_1845+69insGGTGGGGGG
ENST00000245907.10:c.1845+68_1845+69insGGTGGGGGG ENSP00000245907.4:n.1845+68_1845+69insGGTGGGGGG
NM_000064.3:c.1845+68_1845+69insGGTGGGGGG NP_000055.2:n.1845+68_1845+69insGGTGGGGGG
NM_000064.4:c.1845+68_1845+69insGGTGGGGGG MANE Select NP_000055.2:n.1845+68_1845+69insGGTGGGGGG