Canonical Allele Identifier: CA2697556137

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6718376_6718377delinsCT , CM000681.2:g.6718376_6718377delinsCT	GRCh38
NC_000019.9:g.6718387_6718388delinsCT , CM000681.1:g.6718387_6718388delinsCT	GRCh37
NC_000019.8:g.6669387_6669388delinsCT	NCBI36
NG_009557.1:g.7275_7276delinsAG , LRG_27:g.7275_7276delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594936.2:n.364_365delinsAG
ENST00000695652.1:c.180_181delinsAG	ENSP00000512083.1:p.Arg61Gly
ENST00000695693.1:c.303_304delinsAG	ENSP00000512104.1:p.Arg102Gly
ENST00000245907.11:c.303_304delinsAG MANE Select	ENSP00000245907.4:p.Arg102Gly
ENST00000245907.10:c.303_304delinsAG	ENSP00000245907.4:p.Arg102Gly
ENST00000594936.1:n.364_365delinsAG
ENST00000600744.1:c.180_181delinsAG	ENSP00000472044.1:p.Arg61Gly
NM_000064.3:c.303_304delinsAG	NP_000055.2:p.Arg102Gly
NM_000064.4:c.303_304delinsAG MANE Select	NP_000055.2:p.Arg102Gly