Canonical Allele Identifier: CA2587875429

Gene: C3

Linked Data

• gnomAD v4: 19-6697838-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697840del , CM000681.2:g.6697840del	GRCh38
NC_000019.9:g.6697851del , CM000681.1:g.6697851del	GRCh37
NC_000019.8:g.6648851del	NCBI36
NG_009557.1:g.27813del , LRG_27:g.27813del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-45del
ENST00000695652.1:c.2318-45del	ENSP00000512083.1:n.2318-45del
ENST00000695653.1:c.350-45del	ENSP00000512084.1:n.350-45del
ENST00000695654.1:c.1565-45del	ENSP00000512085.1:n.1565-45del
ENST00000695655.1:c.1382-45del	ENSP00000512086.1:n.1382-45del
ENST00000695692.1:n.1805-45del
ENST00000245907.11:c.2441-45del MANE Select	ENSP00000245907.4:n.2441-45del
ENST00000245907.10:c.2441-45del	ENSP00000245907.4:n.2441-45del
ENST00000602053.1:n.489-45del
NM_000064.3:c.2441-45del	NP_000055.2:n.2441-45del
NM_000064.4:c.2441-45del MANE Select	NP_000055.2:n.2441-45del