Canonical Allele Identifier: CA2813446736

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713912_6713913insCCTCCCCCCCCAGCCCCCCACCTGGTCCCATCTCCAGCCCCCCACCTG , CM000681.2:g.6713912_6713913insCCTCCCCCCCCAGCCCCCCACCTGGTCCCATCTCCAGCCCCCCACCTG	GRCh38
NC_000019.9:g.6713923_6713924insCCTCCCCCCCCAGCCCCCCACCTGGTCCCATCTCCAGCCCCCCACCTG , CM000681.1:g.6713923_6713924insCCTCCCCCCCCAGCCCCCCACCTGGTCCCATCTCCAGCCCCCCACCTG	GRCh37
NC_000019.8:g.6664923_6664924insCCTCCCCCCCCAGCCCCCCACCTGGTCCCATCTCCAGCCCCCCACCTG	NCBI36
NG_009557.1:g.11781_11782insGGGAGGCAGGTGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGG , LRG_27:g.11781_11782insGGGAGGCAGGTGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.650+121_650+122insGGGAGGCAGGTGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGG	ENSP00000512083.1:n.650+121_650+122insGGGAGGCAGGTGGGGGGCTGGAG...
ENST00000245907.11:c.773+121_773+122insGGGAGGCAGGTGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGG MANE Select	ENSP00000245907.4:n.773+121_773+122insGGGAGGCAGGTGGGGGGCTGGAG...
ENST00000245907.10:c.773+121_773+122insGGGAGGCAGGTGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGG	ENSP00000245907.4:n.773+121_773+122insGGGAGGCAGGTGGGGGGCTGGAG...
ENST00000595577.1:n.277+121_277+122insGGGAGGCAGGTGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGG
NM_000064.3:c.773+121_773+122insGGGAGGCAGGTGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGG	NP_000055.2:n.773+121_773+122insGGGAGGCAGGTGGGGGGCTGGAGATGGGA...
NM_000064.4:c.773+121_773+122insGGGAGGCAGGTGGGGGGCTGGAGATGGGACCAGGTGGGGGGCTGGGGG MANE Select	NP_000055.2:n.773+121_773+122insGGGAGGCAGGTGGGGGGCTGGAGATGGGA...