Canonical Allele Identifier: CA2320551673
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6682275_6682276delinsGC , CM000681.2:g.6682275_6682276delinsGC GRCh38
NC_000019.9:g.6682286_6682287delinsGC , CM000681.1:g.6682286_6682287delinsGC GRCh37
NC_000019.8:g.6633286_6633287delinsGC NCBI36
NG_009557.1:g.43376_43377delinsGC , LRG_27:g.43376_43377delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.2521-47_2521-46delinsGC
ENST00000695653.1:c.2082-47_2082-46delinsGC ENSP00000512084.1:n.2082-47_2082-46delinsGC
ENST00000695654.1:c.3198-47_3198-46delinsGC ENSP00000512085.1:n.3198-47_3198-46delinsGC
ENST00000695689.1:c.144-47_144-46delinsGC ENSP00000512101.1:n.144-47_144-46delinsGC
ENST00000695690.1:n.364-47_364-46delinsGC
ENST00000695691.1:n.364-47_364-46delinsGC
ENST00000245907.11:c.4173-47_4173-46delinsGC MANE Select ENSP00000245907.4:n.4173-47_4173-46delinsGC
ENST00000245907.10:c.4173-47_4173-46delinsGC ENSP00000245907.4:n.4173-47_4173-46delinsGC
ENST00000596548.1:c.294-47_294-46delinsGC ENSP00000469744.1:n.294-47_294-46delinsGC
ENST00000599899.5:n.1085_1086delinsGC
ENST00000601008.1:c.242-4318_242-4317delinsGC ENSP00000471384.1:n.242-4318_242-4317delinsGC
NM_000064.3:c.4173-47_4173-46delinsGC NP_000055.2:n.4173-47_4173-46delinsGC
NM_000064.4:c.4173-47_4173-46delinsGC MANE Select NP_000055.2:n.4173-47_4173-46delinsGC