Canonical Allele Identifier: CA2587878572
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713907_6713908insCCCTGACTCCACCCCCAGCCCCCCACCTGGTCCCATCTCCAGCCCCCC , CM000681.2:g.6713907_6713908insCCCTGACTCCACCCCCAGCCCCCCACCTGGTCCCATCTCCAGCCCCCC GRCh38
NC_000019.9:g.6713918_6713919insCCCTGACTCCACCCCCAGCCCCCCACCTGGTCCCATCTCCAGCCCCCC , CM000681.1:g.6713918_6713919insCCCTGACTCCACCCCCAGCCCCCCACCTGGTCCCATCTCCAGCCCCCC GRCh37
NC_000019.8:g.6664918_6664919insCCCTGACTCCACCCCCAGCCCCCCACCTGGTCCCATCTCCAGCCCCCC NCBI36
NG_009557.1:g.11791_11792insGGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGG , LRG_27:g.11791_11792insGGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.650+131_650+132insGGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGG ENSP00000512083.1:n.650+131_650+132insGGGGGGGCTGGAGATGGGACCAG...
ENST00000245907.11:c.773+131_773+132insGGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGG MANE Select ENSP00000245907.4:n.773+131_773+132insGGGGGGGCTGGAGATGGGACCAG...
ENST00000245907.10:c.773+131_773+132insGGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGG ENSP00000245907.4:n.773+131_773+132insGGGGGGGCTGGAGATGGGACCAG...
ENST00000595577.1:n.277+131_277+132insGGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGG
NM_000064.3:c.773+131_773+132insGGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGG NP_000055.2:n.773+131_773+132insGGGGGGGCTGGAGATGGGACCAGGTGGGG...
NM_000064.4:c.773+131_773+132insGGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGGTGGAGTCAGG MANE Select NP_000055.2:n.773+131_773+132insGGGGGGGCTGGAGATGGGACCAGGTGGGG...