Canonical Allele Identifier: CA993077831

Gene: C3

Linked Data

• gnomAD v3: 19-6713653-C-CGGTGATGGTGACCT
• gnomAD v4: 19-6713653-C-CGGTGATGGTGACCT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713653_6713654insGGTGATGGTGACCT , CM000681.2:g.6713653_6713654insGGTGATGGTGACCT	GRCh38
NC_000019.9:g.6713664_6713665insGGTGATGGTGACCT , CM000681.1:g.6713664_6713665insGGTGATGGTGACCT	GRCh37
NC_000019.8:g.6664664_6664665insGGTGATGGTGACCT	NCBI36
NG_009557.1:g.11998_11999insAGGTCACCATCACC , LRG_27:g.11998_11999insAGGTCACCATCACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-145_651-144insAGGTCACCATCACC	ENSP00000512083.1:n.651-145_651-144insAGGTCACCATCACC
ENST00000245907.11:c.774-145_774-144insAGGTCACCATCACC MANE Select	ENSP00000245907.4:n.774-145_774-144insAGGTCACCATCACC
ENST00000245907.10:c.774-145_774-144insAGGTCACCATCACC	ENSP00000245907.4:n.774-145_774-144insAGGTCACCATCACC
ENST00000595577.1:n.278-145_278-144insAGGTCACCATCACC
ENST00000597442.5:n.23+112_23+113insAGGTCACCATCACC
NM_000064.3:c.774-145_774-144insAGGTCACCATCACC	NP_000055.2:n.774-145_774-144insAGGTCACCATCACC
NM_000064.4:c.774-145_774-144insAGGTCACCATCACC MANE Select	NP_000055.2:n.774-145_774-144insAGGTCACCATCACC