Canonical Allele Identifier: CA2576592398

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713535dup , CM000681.2:g.6713535dup	GRCh38
NC_000019.9:g.6713546dup , CM000681.1:g.6713546dup	GRCh37
NC_000019.8:g.6664546dup	NCBI36
NG_009557.1:g.12117dup , LRG_27:g.12117dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-26dup	ENSP00000512083.1:n.651-26dup
ENST00000695692.1:n.72dup
ENST00000245907.11:c.774-26dup MANE Select	ENSP00000245907.4:n.774-26dup
ENST00000245907.10:c.774-26dup	ENSP00000245907.4:n.774-26dup
ENST00000595577.1:n.278-26dup
ENST00000597442.5:n.24-26dup
NM_000064.3:c.774-26dup	NP_000055.2:n.774-26dup
NM_000064.4:c.774-26dup MANE Select	NP_000055.2:n.774-26dup