Canonical Allele Identifier: CA2320566094

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710022_6710023delinsAG , CM000681.2:g.6710022_6710023delinsAG	GRCh38
NC_000019.9:g.6710033_6710034delinsAG , CM000681.1:g.6710033_6710034delinsAG	GRCh37
NC_000019.8:g.6661033_6661034delinsAG	NCBI36
NG_009557.1:g.15629_15630delinsCT , LRG_27:g.15629_15630delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-181_1564-180delinsCT	ENSP00000512083.1:n.1564-181_1564-180delinsCT
ENST00000695654.1:c.811-181_811-180delinsCT	ENSP00000512085.1:n.811-181_811-180delinsCT
ENST00000695655.1:c.592-145_592-144delinsCT	ENSP00000512086.1:n.592-145_592-144delinsCT
ENST00000695692.1:n.1051-181_1051-180delinsCT
ENST00000245907.11:c.1687-181_1687-180delinsCT MANE Select	ENSP00000245907.4:n.1687-181_1687-180delinsCT
ENST00000245907.10:c.1687-181_1687-180delinsCT	ENSP00000245907.4:n.1687-181_1687-180delinsCT
ENST00000600763.1:n.320-181_320-180delinsCT
NM_000064.3:c.1687-181_1687-180delinsCT	NP_000055.2:n.1687-181_1687-180delinsCT
NM_000064.4:c.1687-181_1687-180delinsCT MANE Select	NP_000055.2:n.1687-181_1687-180delinsCT