Canonical Allele Identifier: CA993073771
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710051_6710054del , CM000681.2:g.6710051_6710054del GRCh38
NC_000019.9:g.6710062_6710065del , CM000681.1:g.6710062_6710065del GRCh37
NC_000019.8:g.6661062_6661065del NCBI36
NG_009557.1:g.15598_15601del , LRG_27:g.15598_15601del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-212_1564-209del ENSP00000512083.1:n.1564-212_1564-209del
ENST00000695654.1:c.811-212_811-209del ENSP00000512085.1:n.811-212_811-209del
ENST00000695655.1:c.592-176_592-173del ENSP00000512086.1:n.592-176_592-173del
ENST00000695692.1:n.1051-212_1051-209del
ENST00000245907.11:c.1687-212_1687-209del MANE Select ENSP00000245907.4:n.1687-212_1687-209del
ENST00000245907.10:c.1687-212_1687-209del ENSP00000245907.4:n.1687-212_1687-209del
ENST00000600763.1:n.320-212_320-209del
NM_000064.3:c.1687-212_1687-209del NP_000055.2:n.1687-212_1687-209del
NM_000064.4:c.1687-212_1687-209del MANE Select NP_000055.2:n.1687-212_1687-209del