Canonical Allele Identifier: CA993073457
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710000_6710005del , CM000681.2:g.6710000_6710005del GRCh38
NC_000019.9:g.6710011_6710016del , CM000681.1:g.6710011_6710016del GRCh37
NC_000019.8:g.6661011_6661016del NCBI36
NG_009557.1:g.15650_15655del , LRG_27:g.15650_15655del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-160_1564-155del ENSP00000512083.1:n.1564-160_1564-155del
ENST00000695654.1:c.811-160_811-155del ENSP00000512085.1:n.811-160_811-155del
ENST00000695655.1:c.592-124_592-119del ENSP00000512086.1:n.592-124_592-119del
ENST00000695692.1:n.1051-160_1051-155del
ENST00000245907.11:c.1687-160_1687-155del MANE Select ENSP00000245907.4:n.1687-160_1687-155del
ENST00000245907.10:c.1687-160_1687-155del ENSP00000245907.4:n.1687-160_1687-155del
ENST00000600763.1:n.320-160_320-155del
NM_000064.3:c.1687-160_1687-155del NP_000055.2:n.1687-160_1687-155del
NM_000064.4:c.1687-160_1687-155del MANE Select NP_000055.2:n.1687-160_1687-155del