Canonical Allele Identifier: CA2587873425

Gene: C3

Linked Data

• gnomAD v4: 19-6686333-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686333_6686334insA , CM000681.2:g.6686333_6686334insA	GRCh38
NC_000019.9:g.6686344_6686345insA , CM000681.1:g.6686344_6686345insA	GRCh37
NC_000019.8:g.6637344_6637345insA	NCBI36
NG_009557.1:g.39318_39319insT , LRG_27:g.39318_39319insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1995-47_1995-46insT
ENST00000695652.1:c.3524-47_3524-46insT	ENSP00000512083.1:n.3524-47_3524-46insT
ENST00000695653.1:c.1556-47_1556-46insT	ENSP00000512084.1:n.1556-47_1556-46insT
ENST00000695654.1:c.2672-47_2672-46insT	ENSP00000512085.1:n.2672-47_2672-46insT
ENST00000695655.1:c.2588-47_2588-46insT	ENSP00000512086.1:n.2588-47_2588-46insT
ENST00000695692.1:n.3011-47_3011-46insT
ENST00000245907.11:c.3647-47_3647-46insT MANE Select	ENSP00000245907.4:n.3647-47_3647-46insT
ENST00000245907.10:c.3647-47_3647-46insT	ENSP00000245907.4:n.3647-47_3647-46insT
ENST00000596238.1:n.43_44insT
ENST00000598805.2:n.828_829insT
ENST00000601008.1:c.241+412_241+413insT	ENSP00000471384.1:n.241+412_241+413insT
NM_000064.3:c.3647-47_3647-46insT	NP_000055.2:n.3647-47_3647-46insT
NM_000064.4:c.3647-47_3647-46insT MANE Select	NP_000055.2:n.3647-47_3647-46insT