Canonical Allele Identifier: CA2320567671
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6712836_6712837delinsGA , CM000681.2:g.6712836_6712837delinsGA GRCh38
NC_000019.9:g.6712847_6712848delinsGA , CM000681.1:g.6712847_6712848delinsGA GRCh37
NC_000019.8:g.6663847_6663848delinsGA NCBI36
NG_009557.1:g.12815_12816delinsTC , LRG_27:g.12815_12816delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.881-214_881-213delinsTC ENSP00000512083.1:n.881-214_881-213delinsTC
ENST00000695654.1:c.128-214_128-213delinsTC ENSP00000512085.1:n.128-214_128-213delinsTC
ENST00000695692.1:n.328-174_328-173delinsTC
ENST00000245907.11:c.1004-214_1004-213delinsTC MANE Select ENSP00000245907.4:n.1004-214_1004-213delinsTC
ENST00000245907.10:c.1004-214_1004-213delinsTC ENSP00000245907.4:n.1004-214_1004-213delinsTC
ENST00000594270.5:n.128-235_128-234delinsTC
ENST00000595577.1:n.508-214_508-213delinsTC
ENST00000597442.5:n.254-214_254-213delinsTC
NM_000064.3:c.1004-214_1004-213delinsTC NP_000055.2:n.1004-214_1004-213delinsTC
NM_000064.4:c.1004-214_1004-213delinsTC MANE Select NP_000055.2:n.1004-214_1004-213delinsTC