Canonical Allele Identifier: CA358867323

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183684740G>A , CM000666.2:g.183684740G>A	GRCh38
NC_000004.11:g.184605893G>A , CM000666.1:g.184605893G>A	GRCh37
NC_000004.10:g.184842887G>A	NCBI36
NG_033102.1:g.30474G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.1466G>A MANE Select	NP_068761.4:p.Trp489Ter
ENST00000334690.11:c.1466G>A MANE Select	ENSP00000335371.6:p.Trp489Ter
NM_021942.5:c.1466G>A	NP_068761.4:p.Trp489Ter
NM_199053.2:c.1466G>A	NP_951008.1:p.Trp489Ter
NM_199053.3:c.1466G>A	NP_951008.1:p.Trp489Ter
ENST00000334690.10:c.1466G>A	ENSP00000335371.6:p.Trp489Ter
ENST00000357207.8:c.1466G>A	ENSP00000349738.4:p.Trp489Ter
ENST00000505676.5:c.348+734G>A	ENSP00000422915.1:n.348+734G>A
ENST00000512476.1:c.284G>A	ENSP00000421004.1:p.Trp95Ter
XM_011532180.1:c.1466G>A	XP_011530482.1:p.Trp489Ter
XM_017008537.2:c.1466G>A	XP_016864026.1:p.Trp489Ter
XM_017008538.2:c.1466G>A	XP_016864027.1:p.Trp489Ter
XM_024454179.1:c.1466G>A	XP_024309947.1:p.Trp489Ter
XM_024454180.1:c.1466G>A	XP_024309948.1:p.Trp489Ter
XM_024454181.1:c.116G>A	XP_024309949.1:p.Trp39Ter
XR_001741315.2:n.1658G>A