Canonical Allele Identifier: CA6311452

Gene: TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119020256A>G , CM000673.2:g.119020256A>G	GRCh38
NC_000011.9:g.118890966A>G , CM000673.1:g.118890966A>G	GRCh37
NC_000011.8:g.118396176A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016146.6:c.454+3A>G MANE Select	NP_057230.1:n.454+3A>G
ENST00000533632.6:c.454+3A>G MANE Select	ENSP00000436005.1:n.454+3A>G
NM_001318486.1:c.136+939A>G	NP_001305415.1:n.136+939A>G
NM_001318486.2:c.136+939A>G	NP_001305415.1:n.136+939A>G
NM_001318488.1:c.454+3A>G	NP_001305417.1:n.454+3A>G
NM_001318488.2:c.454+3A>G	NP_001305417.1:n.454+3A>G
NM_001318489.1:c.292+3A>G	NP_001305418.1:n.292+3A>G
NM_001318489.2:c.292+3A>G	NP_001305418.1:n.292+3A>G
NM_001318490.1:c.325+3A>G	NP_001305419.1:n.325+3A>G
NM_001318490.2:c.325+3A>G	NP_001305419.1:n.325+3A>G
NM_001318492.1:c.139+3A>G	NP_001305421.1:n.139+3A>G
NM_001318492.2:c.139+3A>G	NP_001305421.1:n.139+3A>G
NM_001318494.1:c.175+1286A>G	NP_001305423.1:n.175+1286A>G
NM_001318494.2:c.175+1286A>G	NP_001305423.1:n.175+1286A>G
NM_016146.4:c.454+3A>G	NP_057230.1:n.454+3A>G
NM_016146.5:c.454+3A>G	NP_057230.1:n.454+3A>G
ENST00000359005.8:c.454+3A>G	ENSP00000351896.4:n.454+3A>G
ENST00000434101.6:c.292+3A>G	ENSP00000405033.2:n.292+3A>G
ENST00000447216.2:n.487A>G
ENST00000525079.5:c.*207+3A>G	ENSP00000433658.1:n.*207+3A>G
ENST00000525303.5:c.175+1286A>G	ENSP00000435339.1:n.175+1286A>G
ENST00000528230.5:c.325+3A>G	ENSP00000436827.1:n.325+3A>G
ENST00000531290.5:n.656+3A>G
ENST00000533012.1:c.350+939A>G	ENSP00000436281.1:n.350+939A>G
ENST00000533058.5:c.454+3A>G	ENSP00000432920.1:n.454+3A>G
ENST00000533149.1:n.862+3A>G
ENST00000533632.5:c.454+3A>G	ENSP00000436005.1:n.454+3A>G
XM_011542867.1:c.139+3A>G	XP_011541169.1:n.139+3A>G
XR_947830.1:n.383+939A>G