Canonical Allele Identifier: CA2813446922
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6718528_6718529insAATCATACGTGAGATTTCCTTGTCCCGACCGATGACTGGTTCTAACTTGCCTGAACGCGCTTGCTCTGTCAAATCATGCGTATA , CM000681.2:g.6718528_6718529insAATCATACGTGAGATTTCCTTGTCCCGACCGATGACTGGTTCTAACTTGCCTGAACGCGCTTGCTCTGTCAAATCATGCGTATA GRCh38
NC_000019.9:g.6718539_6718540insAATCATACGTGAGATTTCCTTGTCCCGACCGATGACTGGTTCTAACTTGCCTGAACGCGCTTGCTCTGTCAAATCATGCGTATA , CM000681.1:g.6718539_6718540insAATCATACGTGAGATTTCCTTGTCCCGACCGATGACTGGTTCTAACTTGCCTGAACGCGCTTGCTCTGTCAAATCATGCGTATA GRCh37
NC_000019.8:g.6669539_6669540insAATCATACGTGAGATTTCCTTGTCCCGACCGATGACTGGTTCTAACTTGCCTGAACGCGCTTGCTCTGTCAAATCATGCGTATA NCBI36
NG_009557.1:g.7123_7124insTATACGCATGATTTGACAGAGCAAGCGCGTTCAGGCAAGTTAGAACCAGTCATCGGTCGGGACAAGGAAATCTCACGTATGATT , LRG_27:g.7123_7124insTATACGCATGATTTGACAGAGCAAGCGCGTTCAGGCAAGTTAGAACCAGTCATCGGTCGGGACAAGGAAATCTCACGTATGATT

Transcript Alleles

HGVS Amino-acid change
ENST00000594936.2:n.329-117_329-116insTATACGCATGATTTGACAGAGCAAGCGCGTTCAGGCAAGTTAGAACCAGTCATCGGTCGGGACAAGGAAATCTCACGTATGATT
ENST00000695652.1:c.145-117_145-116insTATACGCATGATTTGACAGAGCAAGCGCGTTCAGGCAAGTTAGAACCAGTCATCGGTCGGGACAAGGAAATCTCACGTATGATT ENSP00000512083.1:n.145-117_145-116insTATACGCATGATTTGACAGAGCA...
ENST00000695693.1:c.268-117_268-116insTATACGCATGATTTGACAGAGCAAGCGCGTTCAGGCAAGTTAGAACCAGTCATCGGTCGGGACAAGGAAATCTCACGTATGATT ENSP00000512104.1:n.268-117_268-116insTATACGCATGATTTGACAGAGCA...
ENST00000245907.11:c.268-117_268-116insTATACGCATGATTTGACAGAGCAAGCGCGTTCAGGCAAGTTAGAACCAGTCATCGGTCGGGACAAGGAAATCTCACGTATGATT MANE Select ENSP00000245907.4:n.268-117_268-116insTATACGCATGATTTGACAGAGCA...
ENST00000245907.10:c.268-117_268-116insTATACGCATGATTTGACAGAGCAAGCGCGTTCAGGCAAGTTAGAACCAGTCATCGGTCGGGACAAGGAAATCTCACGTATGATT ENSP00000245907.4:n.268-117_268-116insTATACGCATGATTTGACAGAGCA...
ENST00000594936.1:n.329-117_329-116insTATACGCATGATTTGACAGAGCAAGCGCGTTCAGGCAAGTTAGAACCAGTCATCGGTCGGGACAAGGAAATCTCACGTATGATT
ENST00000600744.1:c.145-117_145-116insTATACGCATGATTTGACAGAGCAAGCGCGTTCAGGCAAGTTAGAACCAGTCATCGGTCGGGACAAGGAAATCTCACGTATGATT ENSP00000472044.1:n.145-117_145-116insTATACGCATGATTTGACAGAGCA...
NM_000064.3:c.268-117_268-116insTATACGCATGATTTGACAGAGCAAGCGCGTTCAGGCAAGTTAGAACCAGTCATCGGTCGGGACAAGGAAATCTCACGTATGATT NP_000055.2:n.268-117_268-116insTATACGCATGATTTGACAGAGCAAGCGCG...
NM_000064.4:c.268-117_268-116insTATACGCATGATTTGACAGAGCAAGCGCGTTCAGGCAAGTTAGAACCAGTCATCGGTCGGGACAAGGAAATCTCACGTATGATT MANE Select NP_000055.2:n.268-117_268-116insTATACGCATGATTTGACAGAGCAAGCGCG...