Canonical Allele Identifier: CA358866709

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183684224G>A , CM000666.2:g.183684224G>A	GRCh38
NC_000004.11:g.184605377G>A , CM000666.1:g.184605377G>A	GRCh37
NC_000004.10:g.184842371G>A	NCBI36
NG_033102.1:g.29958G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.1366+1G>A MANE Select	NP_068761.4:n.1366+1G>A
ENST00000334690.11:c.1366+1G>A MANE Select	ENSP00000335371.6:n.1366+1G>A
NM_021942.5:c.1366+1G>A	NP_068761.4:n.1366+1G>A
NM_199053.2:c.1366+1G>A	NP_951008.1:n.1366+1G>A
NM_199053.3:c.1366+1G>A	NP_951008.1:n.1366+1G>A
ENST00000334690.10:c.1366+1G>A	ENSP00000335371.6:n.1366+1G>A
ENST00000357207.8:c.1366+1G>A	ENSP00000349738.4:n.1366+1G>A
ENST00000505676.5:c.348+218G>A	ENSP00000422915.1:n.348+218G>A
ENST00000512476.1:c.184+1G>A	ENSP00000421004.1:n.184+1G>A
XM_011532180.1:c.1366+1G>A	XP_011530482.1:n.1366+1G>A
XM_017008537.2:c.1366+1G>A	XP_016864026.1:n.1366+1G>A
XM_017008538.2:c.1366+1G>A	XP_016864027.1:n.1366+1G>A
XM_024454179.1:c.1366+1G>A	XP_024309947.1:n.1366+1G>A
XM_024454180.1:c.1366+1G>A	XP_024309948.1:n.1366+1G>A
XM_024454181.1:c.16+1G>A	XP_024309949.1:n.16+1G>A
XR_001741315.2:n.1558+1G>A