Canonical Allele Identifier: CA358859148

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183666427G>A , CM000666.2:g.183666427G>A	GRCh38
NC_000004.11:g.184587580G>A , CM000666.1:g.184587580G>A	GRCh37
NC_000004.10:g.184824574G>A	NCBI36
NG_033102.1:g.12161G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.374+1G>A MANE Select	NP_068761.4:n.374+1G>A
ENST00000334690.11:c.374+1G>A MANE Select	ENSP00000335371.6:n.374+1G>A
NM_021942.5:c.374+1G>A	NP_068761.4:n.374+1G>A
NM_199053.2:c.374+1G>A	NP_951008.1:n.374+1G>A
NM_199053.3:c.374+1G>A	NP_951008.1:n.374+1G>A
ENST00000334690.10:c.374+1G>A	ENSP00000335371.6:n.374+1G>A
ENST00000357207.8:c.374+1G>A	ENSP00000349738.4:n.374+1G>A
ENST00000505676.5:c.162+2398G>A	ENSP00000422915.1:n.162+2398G>A
ENST00000509857.5:n.225+1G>A
XM_011532180.1:c.374+1G>A	XP_011530482.1:n.374+1G>A
XM_017008537.2:c.374+1G>A	XP_016864026.1:n.374+1G>A
XM_017008538.2:c.374+1G>A	XP_016864027.1:n.374+1G>A
XM_024454179.1:c.374+1G>A	XP_024309947.1:n.374+1G>A
XM_024454180.1:c.374+1G>A	XP_024309948.1:n.374+1G>A
XM_024454181.1:c.-883+1G>A	XP_024309949.1:n.-883+1G>A
XR_001741315.2:n.566+1G>A