Canonical Allele Identifier: CA2320565892

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709655_6709669delinsCTCAGCAGCCTTGGG , CM000681.2:g.6709655_6709669delinsCTCAGCAGCCTTGGG	GRCh38
NC_000019.9:g.6709666_6709680delinsCTCAGCAGCCTTGGG , CM000681.1:g.6709666_6709680delinsCTCAGCAGCCTTGGG	GRCh37
NC_000019.8:g.6660666_6660680delinsCTCAGCAGCCTTGGG	NCBI36
NG_009557.1:g.15983_15997delinsCCCAAGGCTGCTGAG , LRG_27:g.15983_15997delinsCCCAAGGCTGCTGAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000695652.1:c.1722+15_1722+29delinsCCCAAGGCTGCTGAG	ENSP00000512083.1:n.1722+15_1722+29delins...
ENST00000695654.1:c.969+15_969+29delinsCCCAAGGCTGCTGAG	ENSP00000512085.1:n.969+15_969+29delinsCC...
ENST00000695655.1:c.786+15_786+29delinsCCCAAGGCTGCTGAG	ENSP00000512086.1:n.786+15_786+29delinsCC...
ENST00000695692.1:n.1209+15_1209+29delinsCCCAAGGCTGCTGAG
ENST00000245907.11:c.1845+15_1845+29delinsCCCAAGGCTGCTGAG MANE Select	ENSP00000245907.4:n.1845+15_1845+29delins...
ENST00000245907.10:c.1845+15_1845+29delinsCCCAAGGCTGCTGAG	ENSP00000245907.4:n.1845+15_1845+29delins...
NM_000064.3:c.1845+15_1845+29delinsCCCAAGGCTGCTGAG	NP_000055.2:n.1845+15_1845+29delinsCCCAAG...
NM_000064.4:c.1845+15_1845+29delinsCCCAAGGCTGCTGAG MANE Select	NP_000055.2:n.1845+15_1845+29delinsCCCAAG...