Canonical Allele Identifier: CA2587877592

Gene: C3

Linked Data

• gnomAD v4: 19-6709959-T-TGGGGGGGGGGGGGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709963_6709964insGGGGGGGGGGGGGGGGGGGGGG , CM000681.2:g.6709963_6709964insGGGGGGGGGGGGGGGGGGGGGG	GRCh38
NC_000019.9:g.6709974_6709975insGGGGGGGGGGGGGGGGGGGGGG , CM000681.1:g.6709974_6709975insGGGGGGGGGGGGGGGGGGGGGG	GRCh37
NC_000019.8:g.6660974_6660975insGGGGGGGGGGGGGGGGGGGGGG	NCBI36
NG_009557.1:g.15692_15693insCCCCCCCCCCCCCCCCCCCCCC , LRG_27:g.15692_15693insCCCCCCCCCCCCCCCCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-118_1564-117insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000512083.1:n.1564-118_1564-117insCCCCCCCCCCCCCCCCCCCCC...
ENST00000695654.1:c.811-118_811-117insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000512085.1:n.811-118_811-117insCCCCCCCCCCCCCCCCCCCCCC
ENST00000695655.1:c.592-82_592-81insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000512086.1:n.592-82_592-81insCCCCCCCCCCCCCCCCCCCCCC
ENST00000695692.1:n.1051-118_1051-117insCCCCCCCCCCCCCCCCCCCCCC
ENST00000245907.11:c.1687-118_1687-117insCCCCCCCCCCCCCCCCCCCCCC MANE Select	ENSP00000245907.4:n.1687-118_1687-117insCCCCCCCCCCCCCCCCCCCCC...
ENST00000245907.10:c.1687-118_1687-117insCCCCCCCCCCCCCCCCCCCCCC	ENSP00000245907.4:n.1687-118_1687-117insCCCCCCCCCCCCCCCCCCCCC...
ENST00000600763.1:n.320-118_320-117insCCCCCCCCCCCCCCCCCCCCCC
NM_000064.3:c.1687-118_1687-117insCCCCCCCCCCCCCCCCCCCCCC	NP_000055.2:n.1687-118_1687-117insCCCCCCCCCCCCCCCCCCCCCC
NM_000064.4:c.1687-118_1687-117insCCCCCCCCCCCCCCCCCCCCCC MANE Select	NP_000055.2:n.1687-118_1687-117insCCCCCCCCCCCCCCCCCCCCCC