Canonical Allele Identifier: CA3151571

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183667089T>A , CM000666.2:g.183667089T>A	GRCh38
NC_000004.11:g.184588242T>A , CM000666.1:g.184588242T>A	GRCh37
NC_000004.10:g.184825236T>A	NCBI36
NG_033102.1:g.12823T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.404T>A MANE Select	NP_068761.4:p.Val135Asp
ENST00000334690.11:c.404T>A MANE Select	ENSP00000335371.6:p.Val135Asp
NM_021942.5:c.404T>A	NP_068761.4:p.Val135Asp
NM_199053.2:c.404T>A	NP_951008.1:p.Val135Asp
NM_199053.3:c.404T>A	NP_951008.1:p.Val135Asp
ENST00000334690.10:c.404T>A	ENSP00000335371.6:p.Val135Asp
ENST00000357207.8:c.404T>A	ENSP00000349738.4:p.Val135Asp
ENST00000505676.5:c.162+3060T>A	ENSP00000422915.1:n.162+3060T>A
ENST00000509857.5:n.255T>A
ENST00000511409.1:n.58T>A
ENST00000513600.5:n.197T>A
XM_011532180.1:c.404T>A	XP_011530482.1:p.Val135Asp
XM_017008537.2:c.404T>A	XP_016864026.1:p.Val135Asp
XM_017008538.2:c.404T>A	XP_016864027.1:p.Val135Asp
XM_024454179.1:c.404T>A	XP_024309947.1:p.Val135Asp
XM_024454180.1:c.404T>A	XP_024309948.1:p.Val135Asp
XM_024454181.1:c.-853T>A	XP_024309949.1:n.-853T>A
XR_001741315.2:n.596T>A