Canonical Allele Identifier: CA2587875514
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697939_6697940insTTTGTCGCC , CM000681.2:g.6697939_6697940insTTTGTCGCC GRCh38
NC_000019.9:g.6697950_6697951insTTTGTCGCC , CM000681.1:g.6697950_6697951insTTTGTCGCC GRCh37
NC_000019.8:g.6648950_6648951insTTTGTCGCC NCBI36
NG_009557.1:g.27712_27713insGGCGACAAA , LRG_27:g.27712_27713insGGCGACAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.789-146_789-145insGGCGACAAA
ENST00000695652.1:c.2318-146_2318-145insGGCGACAAA ENSP00000512083.1:n.2318-146_2318-145insGGCGACAAA
ENST00000695653.1:c.350-146_350-145insGGCGACAAA ENSP00000512084.1:n.350-146_350-145insGGCGACAAA
ENST00000695654.1:c.1565-146_1565-145insGGCGACAAA ENSP00000512085.1:n.1565-146_1565-145insGGCGACAAA
ENST00000695655.1:c.1382-146_1382-145insGGCGACAAA ENSP00000512086.1:n.1382-146_1382-145insGGCGACAAA
ENST00000695692.1:n.1805-146_1805-145insGGCGACAAA
ENST00000245907.11:c.2441-146_2441-145insGGCGACAAA MANE Select ENSP00000245907.4:n.2441-146_2441-145insGGCGACAAA
ENST00000245907.10:c.2441-146_2441-145insGGCGACAAA ENSP00000245907.4:n.2441-146_2441-145insGGCGACAAA
ENST00000602053.1:n.489-146_489-145insGGCGACAAA
NM_000064.3:c.2441-146_2441-145insGGCGACAAA NP_000055.2:n.2441-146_2441-145insGGCGACAAA
NM_000064.4:c.2441-146_2441-145insGGCGACAAA MANE Select NP_000055.2:n.2441-146_2441-145insGGCGACAAA