Canonical Allele Identifier: CA6311517

Gene: TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119023290A>G , CM000673.2:g.119023290A>G	GRCh38
NC_000011.9:g.118894000A>G , CM000673.1:g.118894000A>G	GRCh37
NC_000011.8:g.118399210A>G	NCBI36
NG_013331.1:g.12616T>C , LRG_187:g.12616T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_016146.6:c.582-31A>G MANE Select	NP_057230.1:n.582-31A>G
ENST00000533632.6:c.582-31A>G MANE Select	ENSP00000436005.1:n.582-31A>G
NM_001318486.1:c.264-31A>G	NP_001305415.1:n.264-31A>G
NM_001318486.2:c.264-31A>G	NP_001305415.1:n.264-31A>G
NM_001318488.1:c.468-31A>G	NP_001305417.1:n.468-31A>G
NM_001318488.2:c.468-31A>G	NP_001305417.1:n.468-31A>G
NM_001318489.1:c.420-31A>G	NP_001305418.1:n.420-31A>G
NM_001318489.2:c.420-31A>G	NP_001305418.1:n.420-31A>G
NM_001318490.1:c.453-31A>G	NP_001305419.1:n.453-31A>G
NM_001318490.2:c.453-31A>G	NP_001305419.1:n.453-31A>G
NM_001318492.1:c.267-31A>G	NP_001305421.1:n.267-31A>G
NM_001318492.2:c.267-31A>G	NP_001305421.1:n.267-31A>G
NM_001318494.1:c.303-31A>G	NP_001305423.1:n.303-31A>G
NM_001318494.2:c.303-31A>G	NP_001305423.1:n.303-31A>G
NM_016146.4:c.582-31A>G	NP_057230.1:n.582-31A>G
NM_016146.5:c.582-31A>G	NP_057230.1:n.582-31A>G
ENST00000359005.8:c.468-31A>G	ENSP00000351896.4:n.468-31A>G
ENST00000434101.6:c.420-31A>G	ENSP00000405033.2:n.420-31A>G
ENST00000524797.1:n.1571-31A>G
ENST00000525079.5:c.*335-31A>G	ENSP00000433658.1:n.*335-31A>G
ENST00000525303.5:c.303-31A>G	ENSP00000435339.1:n.303-31A>G
ENST00000528230.5:c.453-31A>G	ENSP00000436827.1:n.453-31A>G
ENST00000531290.5:n.784-31A>G
ENST00000533012.1:c.*97-31A>G	ENSP00000436281.1:n.*97-31A>G
ENST00000533058.5:c.581+1404A>G	ENSP00000432920.1:n.581+1404A>G
ENST00000533149.1:n.990-31A>G
ENST00000533632.5:c.582-31A>G	ENSP00000436005.1:n.582-31A>G
XM_011542867.1:c.267-31A>G	XP_011541169.1:n.267-31A>G
XR_947830.1:n.511-31A>G