Canonical Allele Identifier: CA2587877239
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709618_6709619insCCCCCCCCCCCCCCCCCCCCCCC , CM000681.2:g.6709618_6709619insCCCCCCCCCCCCCCCCCCCCCCC GRCh38
NC_000019.9:g.6709629_6709630insCCCCCCCCCCCCCCCCCCCCCCC , CM000681.1:g.6709629_6709630insCCCCCCCCCCCCCCCCCCCCCCC GRCh37
NC_000019.8:g.6660629_6660630insCCCCCCCCCCCCCCCCCCCCCCC NCBI36
NG_009557.1:g.16036_16037insGGGGGGGGGGGGGGGGGGGGGGG , LRG_27:g.16036_16037insGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

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