Canonical Allele Identifier: CA2587871783

Gene: C3

Linked Data

• gnomAD v4: 19-6679324-T-TACCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679324_6679325insACCCA , CM000681.2:g.6679324_6679325insACCCA	GRCh38
NC_000019.9:g.6679335_6679336insACCCA , CM000681.1:g.6679335_6679336insACCCA	GRCh37
NC_000019.8:g.6630335_6630336insACCCA	NCBI36
NG_009557.1:g.46327_46328insTGGGT , LRG_27:g.46327_46328insTGGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2894+82_2894+83insTGGGT
ENST00000695653.1:c.2455+82_2455+83insTGGGT	ENSP00000512084.1:n.2455+82_2455+83insTGGGT
ENST00000695654.1:c.3571+82_3571+83insTGGGT	ENSP00000512085.1:n.3571+82_3571+83insTGGGT
ENST00000695689.1:c.517+82_517+83insTGGGT	ENSP00000512101.1:n.517+82_517+83insTGGGT
ENST00000695690.1:n.1611+82_1611+83insTGGGT
ENST00000695691.1:n.1407+82_1407+83insTGGGT
ENST00000245907.11:c.4546+82_4546+83insTGGGT MANE Select	ENSP00000245907.4:n.4546+82_4546+83insTGGGT
ENST00000245907.10:c.4546+82_4546+83insTGGGT	ENSP00000245907.4:n.4546+82_4546+83insTGGGT
ENST00000599668.1:n.166+57_166+58insTGGGT
ENST00000599899.5:n.1505+82_1505+83insTGGGT
ENST00000601008.1:c.242-1367_242-1366insTGGGT	ENSP00000471384.1:n.242-1367_242-1366insTGGGT
NM_000064.3:c.4546+82_4546+83insTGGGT	NP_000055.2:n.4546+82_4546+83insTGGGT
NM_000064.4:c.4546+82_4546+83insTGGGT MANE Select	NP_000055.2:n.4546+82_4546+83insTGGGT