Canonical Allele Identifier: CA993073353
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709990_6709993del , CM000681.2:g.6709990_6709993del GRCh38
NC_000019.9:g.6710001_6710004del , CM000681.1:g.6710001_6710004del GRCh37
NC_000019.8:g.6661001_6661004del NCBI36
NG_009557.1:g.15661_15664del , LRG_27:g.15661_15664del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-149_1564-146del ENSP00000512083.1:n.1564-149_1564-146del
ENST00000695654.1:c.811-149_811-146del ENSP00000512085.1:n.811-149_811-146del
ENST00000695655.1:c.592-113_592-110del ENSP00000512086.1:n.592-113_592-110del
ENST00000695692.1:n.1051-149_1051-146del
ENST00000245907.11:c.1687-149_1687-146del MANE Select ENSP00000245907.4:n.1687-149_1687-146del
ENST00000245907.10:c.1687-149_1687-146del ENSP00000245907.4:n.1687-149_1687-146del
ENST00000600763.1:n.320-149_320-146del
NM_000064.3:c.1687-149_1687-146del NP_000055.2:n.1687-149_1687-146del
NM_000064.4:c.1687-149_1687-146del MANE Select NP_000055.2:n.1687-149_1687-146del