Canonical Allele Identifier: CA6311436

Gene: TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119020198C>T , CM000673.2:g.119020198C>T	GRCh38
NC_000011.9:g.118890908C>T , CM000673.1:g.118890908C>T	GRCh37
NC_000011.8:g.118396118C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000533632.6:c.399C>T MANE Select	ENSP00000436005.1:p.Gly133=
ENST00000359005.8:c.399C>T	ENSP00000351896.4:p.Gly133=
ENST00000434101.6:c.244-7C>T	ENSP00000405033.2:n.244-7C>T
ENST00000447216.2:n.429C>T
ENST00000525079.5:c.*152C>T	ENSP00000433658.1:n.*152C>T
ENST00000525303.5:c.175+1228C>T	ENSP00000435339.1:n.175+1228C>T
ENST00000528230.5:c.270C>T	ENSP00000436827.1:p.Gly90=
ENST00000531290.5:n.601C>T
ENST00000533012.1:c.350+881C>T	ENSP00000436281.1:n.350+881C>T
ENST00000533058.5:c.399C>T	ENSP00000432920.1:p.Gly133=
ENST00000533149.1:n.807C>T
ENST00000533632.5:c.399C>T	ENSP00000436005.1:p.Gly133=
NM_016146.4:c.399C>T	NP_057230.1:p.Gly133=
XM_011542867.1:c.84C>T	XP_011541169.1:p.Gly28=
XR_947830.1:n.383+881C>T
NM_001318486.1:c.136+881C>T	NP_001305415.1:n.136+881C>T
NM_001318488.1:c.399C>T	NP_001305417.1:p.Gly133=
NM_001318489.1:c.244-7C>T	NP_001305418.1:n.244-7C>T
NM_001318490.1:c.270C>T	NP_001305419.1:p.Gly90=
NM_001318492.1:c.84C>T	NP_001305421.1:p.Gly28=
NM_001318494.1:c.175+1228C>T	NP_001305423.1:n.175+1228C>T
NM_016146.5:c.399C>T	NP_057230.1:p.Gly133=
NM_001318486.2:c.136+881C>T	NP_001305415.1:n.136+881C>T
NM_001318488.2:c.399C>T	NP_001305417.1:p.Gly133=
NM_001318489.2:c.244-7C>T	NP_001305418.1:n.244-7C>T
NM_001318490.2:c.270C>T	NP_001305419.1:p.Gly90=
NM_001318492.2:c.84C>T	NP_001305421.1:p.Gly28=
NM_001318494.2:c.175+1228C>T	NP_001305423.1:n.175+1228C>T
NM_016146.6:c.399C>T MANE Select	NP_057230.1:p.Gly133=