Canonical Allele Identifier: CA920048001

Gene: C3

Linked Data

• dbSNP Id: rs1555685146

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6698005_6698009delinsATAATA , CM000681.2:g.6698005_6698009delinsATAATA	GRCh38
NC_000019.9:g.6698016_6698020delinsATAATA , CM000681.1:g.6698016_6698020delinsATAATA	GRCh37
NC_000019.8:g.6649016_6649020delinsATAATA	NCBI36
NG_009557.1:g.27643_27647delinsTATTAT , LRG_27:g.27643_27647delinsTATTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-215_789-211delinsTATTAT
ENST00000695652.1:c.2318-215_2318-211delinsTATTAT	ENSP00000512083.1:n.2318-215_2318-211delinsTATTAT
ENST00000695653.1:c.350-215_350-211delinsTATTAT	ENSP00000512084.1:n.350-215_350-211delinsTATTAT
ENST00000695654.1:c.1565-215_1565-211delinsTATTAT	ENSP00000512085.1:n.1565-215_1565-211delinsTATTAT
ENST00000695655.1:c.1382-215_1382-211delinsTATTAT	ENSP00000512086.1:n.1382-215_1382-211delinsTATTAT
ENST00000695692.1:n.1805-215_1805-211delinsTATTAT
ENST00000245907.11:c.2441-215_2441-211delinsTATTAT MANE Select	ENSP00000245907.4:n.2441-215_2441-211delinsTATTAT
ENST00000245907.10:c.2441-215_2441-211delinsTATTAT	ENSP00000245907.4:n.2441-215_2441-211delinsTATTAT
ENST00000602053.1:n.489-215_489-211delinsTATTAT
NM_000064.3:c.2441-215_2441-211delinsTATTAT	NP_000055.2:n.2441-215_2441-211delinsTATTAT
NM_000064.4:c.2441-215_2441-211delinsTATTAT MANE Select	NP_000055.2:n.2441-215_2441-211delinsTATTAT