Canonical Allele Identifier: CA2587871934

Gene: C3

Linked Data

• gnomAD v4: 19-6679593-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679593_6679594insA , CM000681.2:g.6679593_6679594insA	GRCh38
NC_000019.9:g.6679604_6679605insA , CM000681.1:g.6679604_6679605insA	GRCh37
NC_000019.8:g.6630604_6630605insA	NCBI36
NG_009557.1:g.46058_46059insT , LRG_27:g.46058_46059insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2805-98_2805-97insT
ENST00000695653.1:c.2366-98_2366-97insT	ENSP00000512084.1:n.2366-98_2366-97insT
ENST00000695654.1:c.3482-98_3482-97insT	ENSP00000512085.1:n.3482-98_3482-97insT
ENST00000695689.1:c.428-98_428-97insT	ENSP00000512101.1:n.428-98_428-97insT
ENST00000695690.1:n.1522-98_1522-97insT
ENST00000695691.1:n.1318-98_1318-97insT
ENST00000245907.11:c.4457-98_4457-97insT MANE Select	ENSP00000245907.4:n.4457-98_4457-97insT
ENST00000245907.10:c.4457-98_4457-97insT	ENSP00000245907.4:n.4457-98_4457-97insT
ENST00000599668.1:n.52-98_52-97insT
ENST00000599899.5:n.1416-98_1416-97insT
ENST00000601008.1:c.242-1636_242-1635insT	ENSP00000471384.1:n.242-1636_242-1635insT
NM_000064.3:c.4457-98_4457-97insT	NP_000055.2:n.4457-98_4457-97insT
NM_000064.4:c.4457-98_4457-97insT MANE Select	NP_000055.2:n.4457-98_4457-97insT