Canonical Allele Identifier: CA993073741
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710046del , CM000681.2:g.6710046del GRCh38
NC_000019.9:g.6710057del , CM000681.1:g.6710057del GRCh37
NC_000019.8:g.6661057del NCBI36
NG_009557.1:g.15606del , LRG_27:g.15606del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-204del ENSP00000512083.1:n.1564-204del
ENST00000695654.1:c.811-204del ENSP00000512085.1:n.811-204del
ENST00000695655.1:c.592-168del ENSP00000512086.1:n.592-168del
ENST00000695692.1:n.1051-204del
ENST00000245907.11:c.1687-204del MANE Select ENSP00000245907.4:n.1687-204del
ENST00000245907.10:c.1687-204del ENSP00000245907.4:n.1687-204del
ENST00000600763.1:n.320-204del
NM_000064.3:c.1687-204del NP_000055.2:n.1687-204del
NM_000064.4:c.1687-204del MANE Select NP_000055.2:n.1687-204del