Canonical Allele Identifier: CA2587878443

Gene: C3

Linked Data

• gnomAD v4: 19-6713652-G-GCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713656_6713657insCCCCCCC , CM000681.2:g.6713656_6713657insCCCCCCC	GRCh38
NC_000019.9:g.6713667_6713668insCCCCCCC , CM000681.1:g.6713667_6713668insCCCCCCC	GRCh37
NC_000019.8:g.6664667_6664668insCCCCCCC	NCBI36
NG_009557.1:g.11999_12000insGGGGGGG , LRG_27:g.11999_12000insGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-144_651-143insGGGGGGG	ENSP00000512083.1:n.651-144_651-143insGGGGGGG
ENST00000245907.11:c.774-144_774-143insGGGGGGG MANE Select	ENSP00000245907.4:n.774-144_774-143insGGGGGGG
ENST00000245907.10:c.774-144_774-143insGGGGGGG	ENSP00000245907.4:n.774-144_774-143insGGGGGGG
ENST00000595577.1:n.278-144_278-143insGGGGGGG
ENST00000597442.5:n.23+113_23+114insGGGGGGG
NM_000064.3:c.774-144_774-143insGGGGGGG	NP_000055.2:n.774-144_774-143insGGGGGGG
NM_000064.4:c.774-144_774-143insGGGGGGG MANE Select	NP_000055.2:n.774-144_774-143insGGGGGGG