Canonical Allele Identifier: CA358874871

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183706941G>A , CM000666.2:g.183706941G>A	GRCh38
NC_000004.11:g.184628094G>A , CM000666.1:g.184628094G>A	GRCh37
NC_000004.10:g.184865088G>A	NCBI36
NG_033102.1:g.52675G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.3189+1G>A MANE Select	NP_068761.4:n.3189+1G>A
ENST00000334690.11:c.3189+1G>A MANE Select	ENSP00000335371.6:n.3189+1G>A
NM_021942.5:c.3189+1G>A	NP_068761.4:n.3189+1G>A
NM_199053.2:c.3189+1G>A	NP_951008.1:n.3189+1G>A
NM_199053.3:c.3189+1G>A	NP_951008.1:n.3189+1G>A
ENST00000334690.10:c.3189+1G>A	ENSP00000335371.6:n.3189+1G>A
ENST00000357207.8:c.3189+1G>A	ENSP00000349738.4:n.3189+1G>A
ENST00000505676.5:c.*1303+1G>A	ENSP00000422915.1:n.*1303+1G>A
ENST00000511955.5:n.1182+1G>A
ENST00000512476.1:c.2007+1G>A	ENSP00000421004.1:n.2007+1G>A
XM_024454179.1:c.3189+1G>A	XP_024309947.1:n.3189+1G>A
XM_024454180.1:c.3189+1G>A	XP_024309948.1:n.3189+1G>A
XM_024454181.1:c.1839+1G>A	XP_024309949.1:n.1839+1G>A
XR_001741315.2:n.3462+1G>A