Canonical Allele Identifier: CA2587871837

Gene: C3

Linked Data

• gnomAD v4: 19-6679376-ACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679378_6679379del , CM000681.2:g.6679378_6679379del	GRCh38
NC_000019.9:g.6679389_6679390del , CM000681.1:g.6679389_6679390del	GRCh37
NC_000019.8:g.6630389_6630390del	NCBI36
NG_009557.1:g.46274_46275del , LRG_27:g.46274_46275del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2894+29_2894+30del
ENST00000695653.1:c.2455+29_2455+30del	ENSP00000512084.1:n.2455+29_2455+30del
ENST00000695654.1:c.3571+29_3571+30del	ENSP00000512085.1:n.3571+29_3571+30del
ENST00000695689.1:c.517+29_517+30del	ENSP00000512101.1:n.517+29_517+30del
ENST00000695690.1:n.1611+29_1611+30del
ENST00000695691.1:n.1407+29_1407+30del
ENST00000245907.11:c.4546+29_4546+30del MANE Select	ENSP00000245907.4:n.4546+29_4546+30del
ENST00000245907.10:c.4546+29_4546+30del	ENSP00000245907.4:n.4546+29_4546+30del
ENST00000599668.1:n.166+4_166+5del
ENST00000599899.5:n.1505+29_1505+30del
ENST00000601008.1:c.242-1420_242-1419del	ENSP00000471384.1:n.242-1420_242-1419del
NM_000064.3:c.4546+29_4546+30del	NP_000055.2:n.4546+29_4546+30del
NM_000064.4:c.4546+29_4546+30del MANE Select	NP_000055.2:n.4546+29_4546+30del