Canonical Allele Identifier: CA2534289696

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709978_6710190del , CM000681.2:g.6709978_6710190del	GRCh38
NC_000019.9:g.6709989_6710201del , CM000681.1:g.6709989_6710201del	GRCh37
NC_000019.8:g.6660989_6661201del	NCBI36
NG_009557.1:g.15473_15685del , LRG_27:g.15473_15685del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-337_1564-125del	ENSP00000512083.1:n.1564-337_1564-125del
ENST00000695654.1:c.811-337_811-125del	ENSP00000512085.1:n.811-337_811-125del
ENST00000695655.1:c.592-301_592-89del	ENSP00000512086.1:n.592-301_592-89del
ENST00000695692.1:n.1051-337_1051-125del
ENST00000245907.11:c.1687-337_1687-125del MANE Select	ENSP00000245907.4:n.1687-337_1687-125del
ENST00000245907.10:c.1687-337_1687-125del	ENSP00000245907.4:n.1687-337_1687-125del
ENST00000600763.1:n.320-337_320-125del
NM_000064.3:c.1687-337_1687-125del	NP_000055.2:n.1687-337_1687-125del
NM_000064.4:c.1687-337_1687-125del MANE Select	NP_000055.2:n.1687-337_1687-125del