Canonical Allele Identifier: CA2320559361

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6698013_6698023delinsATTATTATTAT , CM000681.2:g.6698013_6698023delinsATTATTATTAT	GRCh38
NC_000019.9:g.6698024_6698034delinsATTATTATTAT , CM000681.1:g.6698024_6698034delinsATTATTATTAT	GRCh37
NC_000019.8:g.6649024_6649034delinsATTATTATTAT	NCBI36
NG_009557.1:g.27629_27639delinsATAATAATAAT , LRG_27:g.27629_27639delinsATAATAATAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-229_789-219delinsATAATAATAAT
ENST00000695652.1:c.2318-229_2318-219delinsATAATAATAAT	ENSP00000512083.1:n.2318-229_2318-219delinsATAATAATAAT
ENST00000695653.1:c.350-229_350-219delinsATAATAATAAT	ENSP00000512084.1:n.350-229_350-219delinsATAATAATAAT
ENST00000695654.1:c.1565-229_1565-219delinsATAATAATAAT	ENSP00000512085.1:n.1565-229_1565-219delinsATAATAATAAT
ENST00000695655.1:c.1382-229_1382-219delinsATAATAATAAT	ENSP00000512086.1:n.1382-229_1382-219delinsATAATAATAAT
ENST00000695692.1:n.1805-229_1805-219delinsATAATAATAAT
ENST00000245907.11:c.2441-229_2441-219delinsATAATAATAAT MANE Select	ENSP00000245907.4:n.2441-229_2441-219delinsATAATAATAAT
ENST00000245907.10:c.2441-229_2441-219delinsATAATAATAAT	ENSP00000245907.4:n.2441-229_2441-219delinsATAATAATAAT
ENST00000602053.1:n.489-229_489-219delinsATAATAATAAT
NM_000064.3:c.2441-229_2441-219delinsATAATAATAAT	NP_000055.2:n.2441-229_2441-219delinsATAATAATAAT
NM_000064.4:c.2441-229_2441-219delinsATAATAATAAT MANE Select	NP_000055.2:n.2441-229_2441-219delinsATAATAATAAT