Canonical Allele Identifier: CA2587877668
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710014_6710015insCGGAGAGAGGGAGGGAGAGAGA , CM000681.2:g.6710014_6710015insCGGAGAGAGGGAGGGAGAGAGA GRCh38
NC_000019.9:g.6710025_6710026insCGGAGAGAGGGAGGGAGAGAGA , CM000681.1:g.6710025_6710026insCGGAGAGAGGGAGGGAGAGAGA GRCh37
NC_000019.8:g.6661025_6661026insCGGAGAGAGGGAGGGAGAGAGA NCBI36
NG_009557.1:g.15658_15659insGTCTCTCTCCCTCCCTCTCTCC , LRG_27:g.15658_15659insGTCTCTCTCCCTCCCTCTCTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-152_1564-151insGTCTCTCTCCCTCCCTCTCTCC ENSP00000512083.1:n.1564-152_1564-151insGTCTCTCTCCCTCCCTCTCTC...
ENST00000695654.1:c.811-152_811-151insGTCTCTCTCCCTCCCTCTCTCC ENSP00000512085.1:n.811-152_811-151insGTCTCTCTCCCTCCCTCTCTCC
ENST00000695655.1:c.592-116_592-115insGTCTCTCTCCCTCCCTCTCTCC ENSP00000512086.1:n.592-116_592-115insGTCTCTCTCCCTCCCTCTCTCC
ENST00000695692.1:n.1051-152_1051-151insGTCTCTCTCCCTCCCTCTCTCC
ENST00000245907.11:c.1687-152_1687-151insGTCTCTCTCCCTCCCTCTCTCC MANE Select ENSP00000245907.4:n.1687-152_1687-151insGTCTCTCTCCCTCCCTCTCTC...
ENST00000245907.10:c.1687-152_1687-151insGTCTCTCTCCCTCCCTCTCTCC ENSP00000245907.4:n.1687-152_1687-151insGTCTCTCTCCCTCCCTCTCTC...
ENST00000600763.1:n.320-152_320-151insGTCTCTCTCCCTCCCTCTCTCC
NM_000064.3:c.1687-152_1687-151insGTCTCTCTCCCTCCCTCTCTCC NP_000055.2:n.1687-152_1687-151insGTCTCTCTCCCTCCCTCTCTCC
NM_000064.4:c.1687-152_1687-151insGTCTCTCTCCCTCCCTCTCTCC MANE Select NP_000055.2:n.1687-152_1687-151insGTCTCTCTCCCTCCCTCTCTCC