Canonical Allele Identifier: CA2587877611
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709978_6709985del , CM000681.2:g.6709978_6709985del GRCh38
NC_000019.9:g.6709989_6709996del , CM000681.1:g.6709989_6709996del GRCh37
NC_000019.8:g.6660989_6660996del NCBI36
NG_009557.1:g.15674_15681del , LRG_27:g.15674_15681del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-136_1564-129del ENSP00000512083.1:n.1564-136_1564-129del
ENST00000695654.1:c.811-136_811-129del ENSP00000512085.1:n.811-136_811-129del
ENST00000695655.1:c.592-100_592-93del ENSP00000512086.1:n.592-100_592-93del
ENST00000695692.1:n.1051-136_1051-129del
ENST00000245907.11:c.1687-136_1687-129del MANE Select ENSP00000245907.4:n.1687-136_1687-129del
ENST00000245907.10:c.1687-136_1687-129del ENSP00000245907.4:n.1687-136_1687-129del
ENST00000600763.1:n.320-136_320-129del
NM_000064.3:c.1687-136_1687-129del NP_000055.2:n.1687-136_1687-129del
NM_000064.4:c.1687-136_1687-129del MANE Select NP_000055.2:n.1687-136_1687-129del