Canonical Allele Identifier: CA2320550445
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6679499_6679501delinsGCG , CM000681.2:g.6679499_6679501delinsGCG GRCh38
NC_000019.9:g.6679510_6679512delinsGCG , CM000681.1:g.6679510_6679512delinsGCG GRCh37
NC_000019.8:g.6630510_6630512delinsGCG NCBI36
NG_009557.1:g.46151_46153delinsCGC , LRG_27:g.46151_46153delinsCGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.2805-5_2805-3delinsCGC
ENST00000695653.1:c.2366-5_2366-3delinsCGC ENSP00000512084.1:n.2366-5_2366-3delinsCGC
ENST00000695654.1:c.3482-5_3482-3delinsCGC ENSP00000512085.1:n.3482-5_3482-3delinsCGC
ENST00000695689.1:c.428-5_428-3delinsCGC ENSP00000512101.1:n.428-5_428-3delinsCGC
ENST00000695690.1:n.1522-5_1522-3delinsCGC
ENST00000695691.1:n.1318-5_1318-3delinsCGC
ENST00000245907.11:c.4457-5_4457-3delinsCGC MANE Select ENSP00000245907.4:n.4457-5_4457-3delinsCGC
ENST00000245907.10:c.4457-5_4457-3delinsCGC ENSP00000245907.4:n.4457-5_4457-3delinsCGC
ENST00000599668.1:n.52-5_52-3delinsCGC
ENST00000599899.5:n.1416-5_1416-3delinsCGC
ENST00000601008.1:c.242-1543_242-1541delinsCGC ENSP00000471384.1:n.242-1543_242-1541delinsCGC
NM_000064.3:c.4457-5_4457-3delinsCGC NP_000055.2:n.4457-5_4457-3delinsCGC
NM_000064.4:c.4457-5_4457-3delinsCGC MANE Select NP_000055.2:n.4457-5_4457-3delinsCGC