Canonical Allele Identifier: CA993073603
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710026_6710039del , CM000681.2:g.6710026_6710039del GRCh38
NC_000019.9:g.6710037_6710050del , CM000681.1:g.6710037_6710050del GRCh37
NC_000019.8:g.6661037_6661050del NCBI36
NG_009557.1:g.15614_15627del , LRG_27:g.15614_15627del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-196_1564-183del ENSP00000512083.1:n.1564-196_1564-183del
ENST00000695654.1:c.811-196_811-183del ENSP00000512085.1:n.811-196_811-183del
ENST00000695655.1:c.592-160_592-147del ENSP00000512086.1:n.592-160_592-147del
ENST00000695692.1:n.1051-196_1051-183del
ENST00000245907.11:c.1687-196_1687-183del MANE Select ENSP00000245907.4:n.1687-196_1687-183del
ENST00000245907.10:c.1687-196_1687-183del ENSP00000245907.4:n.1687-196_1687-183del
ENST00000600763.1:n.320-196_320-183del
NM_000064.3:c.1687-196_1687-183del NP_000055.2:n.1687-196_1687-183del
NM_000064.4:c.1687-196_1687-183del MANE Select NP_000055.2:n.1687-196_1687-183del