Canonical Allele Identifier: CA993073509
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710012_6710015del , CM000681.2:g.6710012_6710015del GRCh38
NC_000019.9:g.6710023_6710026del , CM000681.1:g.6710023_6710026del GRCh37
NC_000019.8:g.6661023_6661026del NCBI36
NG_009557.1:g.15642_15645del , LRG_27:g.15642_15645del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-168_1564-165del ENSP00000512083.1:n.1564-168_1564-165del
ENST00000695654.1:c.811-168_811-165del ENSP00000512085.1:n.811-168_811-165del
ENST00000695655.1:c.592-132_592-129del ENSP00000512086.1:n.592-132_592-129del
ENST00000695692.1:n.1051-168_1051-165del
ENST00000245907.11:c.1687-168_1687-165del MANE Select ENSP00000245907.4:n.1687-168_1687-165del
ENST00000245907.10:c.1687-168_1687-165del ENSP00000245907.4:n.1687-168_1687-165del
ENST00000600763.1:n.320-168_320-165del
NM_000064.3:c.1687-168_1687-165del NP_000055.2:n.1687-168_1687-165del
NM_000064.4:c.1687-168_1687-165del MANE Select NP_000055.2:n.1687-168_1687-165del