Canonical Allele Identifier: CA2587877643

Gene: C3

Linked Data

• gnomAD v4: 19-6709990-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709990_6709991insT , CM000681.2:g.6709990_6709991insT	GRCh38
NC_000019.9:g.6710001_6710002insT , CM000681.1:g.6710001_6710002insT	GRCh37
NC_000019.8:g.6661001_6661002insT	NCBI36
NG_009557.1:g.15661_15662insA , LRG_27:g.15661_15662insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-149_1564-148insA	ENSP00000512083.1:n.1564-149_1564-148insA
ENST00000695654.1:c.811-149_811-148insA	ENSP00000512085.1:n.811-149_811-148insA
ENST00000695655.1:c.592-113_592-112insA	ENSP00000512086.1:n.592-113_592-112insA
ENST00000695692.1:n.1051-149_1051-148insA
ENST00000245907.11:c.1687-149_1687-148insA MANE Select	ENSP00000245907.4:n.1687-149_1687-148insA
ENST00000245907.10:c.1687-149_1687-148insA	ENSP00000245907.4:n.1687-149_1687-148insA
ENST00000600763.1:n.320-149_320-148insA
NM_000064.3:c.1687-149_1687-148insA	NP_000055.2:n.1687-149_1687-148insA
NM_000064.4:c.1687-149_1687-148insA MANE Select	NP_000055.2:n.1687-149_1687-148insA