Canonical Allele Identifier: CA993062266
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6698009_6698021del , CM000681.2:g.6698009_6698021del GRCh38
NC_000019.9:g.6698020_6698032del , CM000681.1:g.6698020_6698032del GRCh37
NC_000019.8:g.6649020_6649032del NCBI36
NG_009557.1:g.27632_27644del , LRG_27:g.27632_27644del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.789-226_789-214del
ENST00000695652.1:c.2318-226_2318-214del ENSP00000512083.1:n.2318-226_2318-214del
ENST00000695653.1:c.350-226_350-214del ENSP00000512084.1:n.350-226_350-214del
ENST00000695654.1:c.1565-226_1565-214del ENSP00000512085.1:n.1565-226_1565-214del
ENST00000695655.1:c.1382-226_1382-214del ENSP00000512086.1:n.1382-226_1382-214del
ENST00000695692.1:n.1805-226_1805-214del
ENST00000245907.11:c.2441-226_2441-214del MANE Select ENSP00000245907.4:n.2441-226_2441-214del
ENST00000245907.10:c.2441-226_2441-214del ENSP00000245907.4:n.2441-226_2441-214del
ENST00000602053.1:n.489-226_489-214del
NM_000064.3:c.2441-226_2441-214del NP_000055.2:n.2441-226_2441-214del
NM_000064.4:c.2441-226_2441-214del MANE Select NP_000055.2:n.2441-226_2441-214del