Canonical Allele Identifier: CA2813446712

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713745_6713746insGGCGGTGATGG , CM000681.2:g.6713745_6713746insGGCGGTGATGG	GRCh38
NC_000019.9:g.6713756_6713757insGGCGGTGATGG , CM000681.1:g.6713756_6713757insGGCGGTGATGG	GRCh37
NC_000019.8:g.6664756_6664757insGGCGGTGATGG	NCBI36
NG_009557.1:g.11906_11907insCCATCACCGCC , LRG_27:g.11906_11907insCCATCACCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-237_651-236insCCATCACCGCC	ENSP00000512083.1:n.651-237_651-236insCCATCACCGCC
ENST00000245907.11:c.774-237_774-236insCCATCACCGCC MANE Select	ENSP00000245907.4:n.774-237_774-236insCCATCACCGCC
ENST00000245907.10:c.774-237_774-236insCCATCACCGCC	ENSP00000245907.4:n.774-237_774-236insCCATCACCGCC
ENST00000595577.1:n.278-237_278-236insCCATCACCGCC
ENST00000597442.5:n.23+20_23+21insCCATCACCGCC
NM_000064.3:c.774-237_774-236insCCATCACCGCC	NP_000055.2:n.774-237_774-236insCCATCACCGCC
NM_000064.4:c.774-237_774-236insCCATCACCGCC MANE Select	NP_000055.2:n.774-237_774-236insCCATCACCGCC