Canonical Allele Identifier: CA2320566044

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709966_6709976delinsGGGGAGAGAGA , CM000681.2:g.6709966_6709976delinsGGGGAGAGAGA	GRCh38
NC_000019.9:g.6709977_6709987delinsGGGGAGAGAGA , CM000681.1:g.6709977_6709987delinsGGGGAGAGAGA	GRCh37
NC_000019.8:g.6660977_6660987delinsGGGGAGAGAGA	NCBI36
NG_009557.1:g.15676_15686delinsTCTCTCTCCCC , LRG_27:g.15676_15686delinsTCTCTCTCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-134_1564-124delinsTCTCTCTCCCC	ENSP00000512083.1:n.1564-134_1564-124delinsTCTCTCTCCCC
ENST00000695654.1:c.811-134_811-124delinsTCTCTCTCCCC	ENSP00000512085.1:n.811-134_811-124delinsTCTCTCTCCCC
ENST00000695655.1:c.592-98_592-88delinsTCTCTCTCCCC	ENSP00000512086.1:n.592-98_592-88delinsTCTCTCTCCCC
ENST00000695692.1:n.1051-134_1051-124delinsTCTCTCTCCCC
ENST00000245907.11:c.1687-134_1687-124delinsTCTCTCTCCCC MANE Select	ENSP00000245907.4:n.1687-134_1687-124delinsTCTCTCTCCCC
ENST00000245907.10:c.1687-134_1687-124delinsTCTCTCTCCCC	ENSP00000245907.4:n.1687-134_1687-124delinsTCTCTCTCCCC
ENST00000600763.1:n.320-134_320-124delinsTCTCTCTCCCC
NM_000064.3:c.1687-134_1687-124delinsTCTCTCTCCCC	NP_000055.2:n.1687-134_1687-124delinsTCTCTCTCCCC
NM_000064.4:c.1687-134_1687-124delinsTCTCTCTCCCC MANE Select	NP_000055.2:n.1687-134_1687-124delinsTCTCTCTCCCC