Canonical Allele Identifier: CA2587876997

Gene: C3

Linked Data

• gnomAD v4: 19-6709611-T-TGGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709611_6709612insGGCC , CM000681.2:g.6709611_6709612insGGCC	GRCh38
NC_000019.9:g.6709622_6709623insGGCC , CM000681.1:g.6709622_6709623insGGCC	GRCh37
NC_000019.8:g.6660622_6660623insGGCC	NCBI36
NG_009557.1:g.16040_16041insGGCC , LRG_27:g.16040_16041insGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1722+72_1722+73insGGCC	ENSP00000512083.1:n.1722+72_1722+73insGGCC
ENST00000695654.1:c.969+72_969+73insGGCC	ENSP00000512085.1:n.969+72_969+73insGGCC
ENST00000695655.1:c.786+72_786+73insGGCC	ENSP00000512086.1:n.786+72_786+73insGGCC
ENST00000695692.1:n.1209+72_1209+73insGGCC
ENST00000245907.11:c.1845+72_1845+73insGGCC MANE Select	ENSP00000245907.4:n.1845+72_1845+73insGGCC
ENST00000245907.10:c.1845+72_1845+73insGGCC	ENSP00000245907.4:n.1845+72_1845+73insGGCC
NM_000064.3:c.1845+72_1845+73insGGCC	NP_000055.2:n.1845+72_1845+73insGGCC
NM_000064.4:c.1845+72_1845+73insGGCC MANE Select	NP_000055.2:n.1845+72_1845+73insGGCC