Canonical Allele Identifier: CA2587878566
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713859_6713860insCCCTGACTCCACCCCCAGCCCCCCACCTGGTCCCATCTCCAGCCCCCC , CM000681.2:g.6713859_6713860insCCCTGACTCCACCCCCAGCCCCCCACCTGGTCCCATCTCCAGCCCCCC GRCh38
NC_000019.9:g.6713870_6713871insCCCTGACTCCACCCCCAGCCCCCCACCTGGTCCCATCTCCAGCCCCCC , CM000681.1:g.6713870_6713871insCCCTGACTCCACCCCCAGCCCCCCACCTGGTCCCATCTCCAGCCCCCC GRCh37
NC_000019.8:g.6664870_6664871insCCCTGACTCCACCCCCAGCCCCCCACCTGGTCCCATCTCCAGCCCCCC NCBI36
NG_009557.1:g.11802_11803insAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGGGGGGGGGCTGG , LRG_27:g.11802_11803insAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGGGGGGGGGCTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.650+142_650+143insAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGGGGGGGGGCTGG ENSP00000512083.1:n.650+142_650+143insAGATGGGACCAGGTGGGGGGCTG...
ENST00000245907.11:c.773+142_773+143insAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGGGGGGGGGCTGG MANE Select ENSP00000245907.4:n.773+142_773+143insAGATGGGACCAGGTGGGGGGCTG...
ENST00000245907.10:c.773+142_773+143insAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGGGGGGGGGCTGG ENSP00000245907.4:n.773+142_773+143insAGATGGGACCAGGTGGGGGGCTG...
ENST00000595577.1:n.277+142_277+143insAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGGGGGGGGGCTGG
NM_000064.3:c.773+142_773+143insAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGGGGGGGGGCTGG NP_000055.2:n.773+142_773+143insAGATGGGACCAGGTGGGGGGCTGGGGGTG...
NM_000064.4:c.773+142_773+143insAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGGGGGGGGGCTGG MANE Select NP_000055.2:n.773+142_773+143insAGATGGGACCAGGTGGGGGGCTGGGGGTG...