Canonical Allele Identifier: CA2320567872
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713337_6713339delinsCAG , CM000681.2:g.6713337_6713339delinsCAG GRCh38
NC_000019.9:g.6713348_6713350delinsCAG , CM000681.1:g.6713348_6713350delinsCAG GRCh37
NC_000019.8:g.6664348_6664350delinsCAG NCBI36
NG_009557.1:g.12313_12315delinsCTG , LRG_27:g.12313_12315delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.754-24_754-22delinsCTG ENSP00000512083.1:n.754-24_754-22delinsCTG
ENST00000695692.1:n.201-24_201-22delinsCTG
ENST00000245907.11:c.877-24_877-22delinsCTG MANE Select ENSP00000245907.4:n.877-24_877-22delinsCTG
ENST00000245907.10:c.877-24_877-22delinsCTG ENSP00000245907.4:n.877-24_877-22delinsCTG
ENST00000595577.1:n.381-24_381-22delinsCTG
ENST00000597442.5:n.127-24_127-22delinsCTG
NM_000064.3:c.877-24_877-22delinsCTG NP_000055.2:n.877-24_877-22delinsCTG
NM_000064.4:c.877-24_877-22delinsCTG MANE Select NP_000055.2:n.877-24_877-22delinsCTG