Canonical Allele Identifier: CA2813446920

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6718527_6718528insCTCAAAATTT , CM000681.2:g.6718527_6718528insCTCAAAATTT	GRCh38
NC_000019.9:g.6718538_6718539insCTCAAAATTT , CM000681.1:g.6718538_6718539insCTCAAAATTT	GRCh37
NC_000019.8:g.6669538_6669539insCTCAAAATTT	NCBI36
NG_009557.1:g.7124_7125insAAATTTTGAG , LRG_27:g.7124_7125insAAATTTTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594936.2:n.329-116_329-115insAAATTTTGAG
ENST00000695652.1:c.145-116_145-115insAAATTTTGAG	ENSP00000512083.1:n.145-116_145-115insAAATTTTGAG
ENST00000695693.1:c.268-116_268-115insAAATTTTGAG	ENSP00000512104.1:n.268-116_268-115insAAATTTTGAG
ENST00000245907.11:c.268-116_268-115insAAATTTTGAG MANE Select	ENSP00000245907.4:n.268-116_268-115insAAATTTTGAG
ENST00000245907.10:c.268-116_268-115insAAATTTTGAG	ENSP00000245907.4:n.268-116_268-115insAAATTTTGAG
ENST00000594936.1:n.329-116_329-115insAAATTTTGAG
ENST00000600744.1:c.145-116_145-115insAAATTTTGAG	ENSP00000472044.1:n.145-116_145-115insAAATTTTGAG
NM_000064.3:c.268-116_268-115insAAATTTTGAG	NP_000055.2:n.268-116_268-115insAAATTTTGAG
NM_000064.4:c.268-116_268-115insAAATTTTGAG MANE Select	NP_000055.2:n.268-116_268-115insAAATTTTGAG