Canonical Allele Identifier: CA2587877294
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709618_6709619insCCCCCCCCCCCCCCCCCCCCCCCT , CM000681.2:g.6709618_6709619insCCCCCCCCCCCCCCCCCCCCCCCT GRCh38
NC_000019.9:g.6709629_6709630insCCCCCCCCCCCCCCCCCCCCCCCT , CM000681.1:g.6709629_6709630insCCCCCCCCCCCCCCCCCCCCCCCT GRCh37
NC_000019.8:g.6660629_6660630insCCCCCCCCCCCCCCCCCCCCCCCT NCBI36
NG_009557.1:g.16033_16034insAGGGGGGGGGGGGGGGGGGGGGGG , LRG_27:g.16033_16034insAGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1722+65_1722+66insAGGGGGGGGGGGGGGGGGGGGGGG ENSP00000512083.1:n.1722+65_1722+66insAGGGGGGGGGGGGGGGGGGGGGG...
ENST00000695654.1:c.969+65_969+66insAGGGGGGGGGGGGGGGGGGGGGGG ENSP00000512085.1:n.969+65_969+66insAGGGGGGGGGGGGGGGGGGGGGGG
ENST00000695655.1:c.786+65_786+66insAGGGGGGGGGGGGGGGGGGGGGGG ENSP00000512086.1:n.786+65_786+66insAGGGGGGGGGGGGGGGGGGGGGGG
ENST00000695692.1:n.1209+65_1209+66insAGGGGGGGGGGGGGGGGGGGGGGG
ENST00000245907.11:c.1845+65_1845+66insAGGGGGGGGGGGGGGGGGGGGGGG MANE Select ENSP00000245907.4:n.1845+65_1845+66insAGGGGGGGGGGGGGGGGGGGGGG...
ENST00000245907.10:c.1845+65_1845+66insAGGGGGGGGGGGGGGGGGGGGGGG ENSP00000245907.4:n.1845+65_1845+66insAGGGGGGGGGGGGGGGGGGGGGG...
NM_000064.3:c.1845+65_1845+66insAGGGGGGGGGGGGGGGGGGGGGGG NP_000055.2:n.1845+65_1845+66insAGGGGGGGGGGGGGGGGGGGGGGG
NM_000064.4:c.1845+65_1845+66insAGGGGGGGGGGGGGGGGGGGGGGG MANE Select NP_000055.2:n.1845+65_1845+66insAGGGGGGGGGGGGGGGGGGGGGGG