Canonical Allele Identifier: CA2587878444
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713656_6713657insCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC , CM000681.2:g.6713656_6713657insCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC GRCh38
NC_000019.9:g.6713667_6713668insCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC , CM000681.1:g.6713667_6713668insCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC GRCh37
NC_000019.8:g.6664667_6664668insCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC NCBI36
NG_009557.1:g.11999_12000insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG , LRG_27:g.11999_12000insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-144_651-143insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000512083.1:n.651-144_651-143insGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000245907.11:c.774-144_774-143insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select ENSP00000245907.4:n.774-144_774-143insGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000245907.10:c.774-144_774-143insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG ENSP00000245907.4:n.774-144_774-143insGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000595577.1:n.278-144_278-143insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000597442.5:n.23+113_23+114insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG
NM_000064.3:c.774-144_774-143insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NP_000055.2:n.774-144_774-143insGGGGGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_000064.4:c.774-144_774-143insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select NP_000055.2:n.774-144_774-143insGGGGGGGGGGGGGGGGGGGGGGGGGGGGG...