Canonical Allele Identifier: CA2582310852
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710015_6710016insAA , CM000681.2:g.6710015_6710016insAA GRCh38
NC_000019.9:g.6710026_6710027insAA , CM000681.1:g.6710026_6710027insAA GRCh37
NC_000019.8:g.6661026_6661027insAA NCBI36
NG_009557.1:g.15636_15637insTT , LRG_27:g.15636_15637insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-174_1564-173insTT ENSP00000512083.1:n.1564-174_1564-173insTT
ENST00000695654.1:c.811-174_811-173insTT ENSP00000512085.1:n.811-174_811-173insTT
ENST00000695655.1:c.592-138_592-137insTT ENSP00000512086.1:n.592-138_592-137insTT
ENST00000695692.1:n.1051-174_1051-173insTT
ENST00000245907.11:c.1687-174_1687-173insTT MANE Select ENSP00000245907.4:n.1687-174_1687-173insTT
ENST00000245907.10:c.1687-174_1687-173insTT ENSP00000245907.4:n.1687-174_1687-173insTT
ENST00000600763.1:n.320-174_320-173insTT
NM_000064.3:c.1687-174_1687-173insTT NP_000055.2:n.1687-174_1687-173insTT
NM_000064.4:c.1687-174_1687-173insTT MANE Select NP_000055.2:n.1687-174_1687-173insTT