Canonical Allele Identifier: CA2320559366

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6698016_6698023delinsATTATTAT , CM000681.2:g.6698016_6698023delinsATTATTAT	GRCh38
NC_000019.9:g.6698027_6698034delinsATTATTAT , CM000681.1:g.6698027_6698034delinsATTATTAT	GRCh37
NC_000019.8:g.6649027_6649034delinsATTATTAT	NCBI36
NG_009557.1:g.27629_27636delinsATAATAAT , LRG_27:g.27629_27636delinsATAATAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-229_789-222delinsATAATAAT
ENST00000695652.1:c.2318-229_2318-222delinsATAATAAT	ENSP00000512083.1:n.2318-229_2318-222delinsATAATAAT
ENST00000695653.1:c.350-229_350-222delinsATAATAAT	ENSP00000512084.1:n.350-229_350-222delinsATAATAAT
ENST00000695654.1:c.1565-229_1565-222delinsATAATAAT	ENSP00000512085.1:n.1565-229_1565-222delinsATAATAAT
ENST00000695655.1:c.1382-229_1382-222delinsATAATAAT	ENSP00000512086.1:n.1382-229_1382-222delinsATAATAAT
ENST00000695692.1:n.1805-229_1805-222delinsATAATAAT
ENST00000245907.11:c.2441-229_2441-222delinsATAATAAT MANE Select	ENSP00000245907.4:n.2441-229_2441-222delinsATAATAAT
ENST00000245907.10:c.2441-229_2441-222delinsATAATAAT	ENSP00000245907.4:n.2441-229_2441-222delinsATAATAAT
ENST00000602053.1:n.489-229_489-222delinsATAATAAT
NM_000064.3:c.2441-229_2441-222delinsATAATAAT	NP_000055.2:n.2441-229_2441-222delinsATAATAAT
NM_000064.4:c.2441-229_2441-222delinsATAATAAT MANE Select	NP_000055.2:n.2441-229_2441-222delinsATAATAAT