Canonical Allele Identifier: CA2587871927

Gene: C3

Linked Data

• gnomAD v4: 19-6679579-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679580_6679581del , CM000681.2:g.6679580_6679581del	GRCh38
NC_000019.9:g.6679591_6679592del , CM000681.1:g.6679591_6679592del	GRCh37
NC_000019.8:g.6630591_6630592del	NCBI36
NG_009557.1:g.46071_46072del , LRG_27:g.46071_46072del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2805-85_2805-84del
ENST00000695653.1:c.2366-85_2366-84del	ENSP00000512084.1:n.2366-85_2366-84del
ENST00000695654.1:c.3482-85_3482-84del	ENSP00000512085.1:n.3482-85_3482-84del
ENST00000695689.1:c.428-85_428-84del	ENSP00000512101.1:n.428-85_428-84del
ENST00000695690.1:n.1522-85_1522-84del
ENST00000695691.1:n.1318-85_1318-84del
ENST00000245907.11:c.4457-85_4457-84del MANE Select	ENSP00000245907.4:n.4457-85_4457-84del
ENST00000245907.10:c.4457-85_4457-84del	ENSP00000245907.4:n.4457-85_4457-84del
ENST00000599668.1:n.52-85_52-84del
ENST00000599899.5:n.1416-85_1416-84del
ENST00000601008.1:c.242-1623_242-1622del	ENSP00000471384.1:n.242-1623_242-1622del
NM_000064.3:c.4457-85_4457-84del	NP_000055.2:n.4457-85_4457-84del
NM_000064.4:c.4457-85_4457-84del MANE Select	NP_000055.2:n.4457-85_4457-84del