Canonical Allele Identifier: CA2320550532
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6679663_6679664delinsGA , CM000681.2:g.6679663_6679664delinsGA GRCh38
NC_000019.9:g.6679674_6679675delinsGA , CM000681.1:g.6679674_6679675delinsGA GRCh37
NC_000019.8:g.6630674_6630675delinsGA NCBI36
NG_009557.1:g.45988_45989delinsTC , LRG_27:g.45988_45989delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.2805-168_2805-167delinsTC
ENST00000695653.1:c.2366-168_2366-167delinsTC ENSP00000512084.1:n.2366-168_2366-167delinsTC
ENST00000695654.1:c.3482-168_3482-167delinsTC ENSP00000512085.1:n.3482-168_3482-167delinsTC
ENST00000695689.1:c.428-168_428-167delinsTC ENSP00000512101.1:n.428-168_428-167delinsTC
ENST00000695690.1:n.1522-168_1522-167delinsTC
ENST00000695691.1:n.1318-168_1318-167delinsTC
ENST00000245907.11:c.4457-168_4457-167delinsTC MANE Select ENSP00000245907.4:n.4457-168_4457-167delinsTC
ENST00000245907.10:c.4457-168_4457-167delinsTC ENSP00000245907.4:n.4457-168_4457-167delinsTC
ENST00000599668.1:n.52-168_52-167delinsTC
ENST00000599899.5:n.1416-168_1416-167delinsTC
ENST00000601008.1:c.242-1706_242-1705delinsTC ENSP00000471384.1:n.242-1706_242-1705delinsTC
NM_000064.3:c.4457-168_4457-167delinsTC NP_000055.2:n.4457-168_4457-167delinsTC
NM_000064.4:c.4457-168_4457-167delinsTC MANE Select NP_000055.2:n.4457-168_4457-167delinsTC