Canonical Allele Identifier: CA2320567975

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713543_6713546delinsCCCT , CM000681.2:g.6713543_6713546delinsCCCT	GRCh38
NC_000019.9:g.6713554_6713557delinsCCCT , CM000681.1:g.6713554_6713557delinsCCCT	GRCh37
NC_000019.8:g.6664554_6664557delinsCCCT	NCBI36
NG_009557.1:g.12106_12109delinsAGGG , LRG_27:g.12106_12109delinsAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-37_651-34delinsAGGG	ENSP00000512083.1:n.651-37_651-34delinsAGGG
ENST00000695692.1:n.61_64delinsAGGG
ENST00000245907.11:c.774-37_774-34delinsAGGG MANE Select	ENSP00000245907.4:n.774-37_774-34delinsAGGG
ENST00000245907.10:c.774-37_774-34delinsAGGG	ENSP00000245907.4:n.774-37_774-34delinsAGGG
ENST00000595577.1:n.278-37_278-34delinsAGGG
ENST00000597442.5:n.24-37_24-34delinsAGGG
NM_000064.3:c.774-37_774-34delinsAGGG	NP_000055.2:n.774-37_774-34delinsAGGG
NM_000064.4:c.774-37_774-34delinsAGGG MANE Select	NP_000055.2:n.774-37_774-34delinsAGGG