Canonical Allele Identifier: CA13399222

Gene: TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119023168T>C , CM000673.2:g.119023168T>C	GRCh38
NC_000011.9:g.118893878T>C , CM000673.1:g.118893878T>C	GRCh37
NC_000011.8:g.118399088T>C	NCBI36
NG_013331.1:g.12738A>G , LRG_187:g.12738A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016146.6:c.582-153T>C MANE Select	NP_057230.1:n.582-153T>C
ENST00000533632.6:c.582-153T>C MANE Select	ENSP00000436005.1:n.582-153T>C
NM_001318486.1:c.264-153T>C	NP_001305415.1:n.264-153T>C
NM_001318486.2:c.264-153T>C	NP_001305415.1:n.264-153T>C
NM_001318488.1:c.468-153T>C	NP_001305417.1:n.468-153T>C
NM_001318488.2:c.468-153T>C	NP_001305417.1:n.468-153T>C
NM_001318489.1:c.420-153T>C	NP_001305418.1:n.420-153T>C
NM_001318489.2:c.420-153T>C	NP_001305418.1:n.420-153T>C
NM_001318490.1:c.453-153T>C	NP_001305419.1:n.453-153T>C
NM_001318490.2:c.453-153T>C	NP_001305419.1:n.453-153T>C
NM_001318492.1:c.267-153T>C	NP_001305421.1:n.267-153T>C
NM_001318492.2:c.267-153T>C	NP_001305421.1:n.267-153T>C
NM_001318494.1:c.303-153T>C	NP_001305423.1:n.303-153T>C
NM_001318494.2:c.303-153T>C	NP_001305423.1:n.303-153T>C
NM_016146.4:c.582-153T>C	NP_057230.1:n.582-153T>C
NM_016146.5:c.582-153T>C	NP_057230.1:n.582-153T>C
ENST00000359005.8:c.468-153T>C	ENSP00000351896.4:n.468-153T>C
ENST00000434101.6:c.420-153T>C	ENSP00000405033.2:n.420-153T>C
ENST00000524797.1:n.1571-153T>C
ENST00000525079.5:c.*335-153T>C	ENSP00000433658.1:n.*335-153T>C
ENST00000525303.5:c.303-153T>C	ENSP00000435339.1:n.303-153T>C
ENST00000526141.1:n.278T>C
ENST00000528230.5:c.453-153T>C	ENSP00000436827.1:n.453-153T>C
ENST00000531290.5:n.784-153T>C
ENST00000533012.1:c.*97-153T>C	ENSP00000436281.1:n.*97-153T>C
ENST00000533058.5:c.581+1282T>C	ENSP00000432920.1:n.581+1282T>C
ENST00000533149.1:n.990-153T>C
ENST00000533632.5:c.582-153T>C	ENSP00000436005.1:n.582-153T>C
XM_011542867.1:c.267-153T>C	XP_011541169.1:n.267-153T>C
XR_947830.1:n.511-153T>C