Canonical Allele Identifier: CA3152207

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183694038G>A , CM000666.2:g.183694038G>A	GRCh38
NC_000004.11:g.184615191G>A , CM000666.1:g.184615191G>A	GRCh37
NC_000004.10:g.184852185G>A	NCBI36
NG_033102.1:g.39772G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.2508G>A MANE Select	NP_068761.4:p.Gln836=
ENST00000334690.11:c.2508G>A MANE Select	ENSP00000335371.6:p.Gln836=
NM_021942.5:c.2508G>A	NP_068761.4:p.Gln836=
NM_199053.2:c.2508G>A	NP_951008.1:p.Gln836=
NM_199053.3:c.2508G>A	NP_951008.1:p.Gln836=
ENST00000334690.10:c.2508G>A	ENSP00000335371.6:p.Gln836=
ENST00000357207.8:c.2508G>A	ENSP00000349738.4:p.Gln836=
ENST00000505676.5:c.*622G>A	ENSP00000422915.1:n.*622G>A
ENST00000512476.1:c.1326G>A	ENSP00000421004.1:p.Gln442=
XM_011532180.1:c.2508G>A	XP_011530482.1:p.Gln836=
XM_017008537.2:c.2508G>A	XP_016864026.1:p.Gln836=
XM_017008538.2:c.2508G>A	XP_016864027.1:p.Gln836=
XM_024454179.1:c.2508G>A	XP_024309947.1:p.Gln836=
XM_024454180.1:c.2508G>A	XP_024309948.1:p.Gln836=
XM_024454181.1:c.1158G>A	XP_024309949.1:p.Gln386=
XR_001741315.2:n.2700G>A