Canonical Allele Identifier: CA2587873423

Gene: C3

Linked Data

• gnomAD v4: 19-6686327-GTCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686328_6686330del , CM000681.2:g.6686328_6686330del	GRCh38
NC_000019.9:g.6686339_6686341del , CM000681.1:g.6686339_6686341del	GRCh37
NC_000019.8:g.6637339_6637341del	NCBI36
NG_009557.1:g.39322_39324del , LRG_27:g.39322_39324del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1995-43_1995-41del
ENST00000695652.1:c.3524-43_3524-41del	ENSP00000512083.1:n.3524-43_3524-41del
ENST00000695653.1:c.1556-43_1556-41del	ENSP00000512084.1:n.1556-43_1556-41del
ENST00000695654.1:c.2672-43_2672-41del	ENSP00000512085.1:n.2672-43_2672-41del
ENST00000695655.1:c.2588-43_2588-41del	ENSP00000512086.1:n.2588-43_2588-41del
ENST00000695692.1:n.3011-43_3011-41del
ENST00000245907.11:c.3647-43_3647-41del MANE Select	ENSP00000245907.4:n.3647-43_3647-41del
ENST00000245907.10:c.3647-43_3647-41del	ENSP00000245907.4:n.3647-43_3647-41del
ENST00000596238.1:n.47_49del
ENST00000598805.2:n.832_834del
ENST00000601008.1:c.241+416_241+418del	ENSP00000471384.1:n.241+416_241+418del
NM_000064.3:c.3647-43_3647-41del	NP_000055.2:n.3647-43_3647-41del
NM_000064.4:c.3647-43_3647-41del MANE Select	NP_000055.2:n.3647-43_3647-41del