Canonical Allele Identifier: CA2587877664
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710013_6710014insTGGGAGAGAGGGAGGGAGAGAG , CM000681.2:g.6710013_6710014insTGGGAGAGAGGGAGGGAGAGAG GRCh38
NC_000019.9:g.6710024_6710025insTGGGAGAGAGGGAGGGAGAGAG , CM000681.1:g.6710024_6710025insTGGGAGAGAGGGAGGGAGAGAG GRCh37
NC_000019.8:g.6661024_6661025insTGGGAGAGAGGGAGGGAGAGAG NCBI36
NG_009557.1:g.15659_15660insACTCTCTCCCTCCCTCTCTCCC , LRG_27:g.15659_15660insACTCTCTCCCTCCCTCTCTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-151_1564-150insACTCTCTCCCTCCCTCTCTCCC ENSP00000512083.1:n.1564-151_1564-150insACTCTCTCCCTCCCTCTCTCC...
ENST00000695654.1:c.811-151_811-150insACTCTCTCCCTCCCTCTCTCCC ENSP00000512085.1:n.811-151_811-150insACTCTCTCCCTCCCTCTCTCCC
ENST00000695655.1:c.592-115_592-114insACTCTCTCCCTCCCTCTCTCCC ENSP00000512086.1:n.592-115_592-114insACTCTCTCCCTCCCTCTCTCCC
ENST00000695692.1:n.1051-151_1051-150insACTCTCTCCCTCCCTCTCTCCC
ENST00000245907.11:c.1687-151_1687-150insACTCTCTCCCTCCCTCTCTCCC MANE Select ENSP00000245907.4:n.1687-151_1687-150insACTCTCTCCCTCCCTCTCTCC...
ENST00000245907.10:c.1687-151_1687-150insACTCTCTCCCTCCCTCTCTCCC ENSP00000245907.4:n.1687-151_1687-150insACTCTCTCCCTCCCTCTCTCC...
ENST00000600763.1:n.320-151_320-150insACTCTCTCCCTCCCTCTCTCCC
NM_000064.3:c.1687-151_1687-150insACTCTCTCCCTCCCTCTCTCCC NP_000055.2:n.1687-151_1687-150insACTCTCTCCCTCCCTCTCTCCC
NM_000064.4:c.1687-151_1687-150insACTCTCTCCCTCCCTCTCTCCC MANE Select NP_000055.2:n.1687-151_1687-150insACTCTCTCCCTCCCTCTCTCCC