Canonical Allele Identifier: CA111861591

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183697763A>G , CM000666.2:g.183697763A>G	GRCh38
NC_000004.11:g.184618916A>G , CM000666.1:g.184618916A>G	GRCh37
NC_000004.10:g.184855910A>G	NCBI36
NG_033102.1:g.43497A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.2779A>G MANE Select	NP_068761.4:p.Ile927Val
ENST00000334690.11:c.2779A>G MANE Select	ENSP00000335371.6:p.Ile927Val
NM_021942.5:c.2779A>G	NP_068761.4:p.Ile927Val
NM_199053.2:c.2779A>G	NP_951008.1:p.Ile927Val
NM_199053.3:c.2779A>G	NP_951008.1:p.Ile927Val
ENST00000334690.10:c.2779A>G	ENSP00000335371.6:p.Ile927Val
ENST00000357207.8:c.2779A>G	ENSP00000349738.4:p.Ile927Val
ENST00000505676.5:c.*893A>G	ENSP00000422915.1:n.*893A>G
ENST00000512476.1:c.1597A>G	ENSP00000421004.1:p.Ile533Val
XM_011532180.1:c.2779A>G	XP_011530482.1:p.Ile927Val
XM_017008537.2:c.2779A>G	XP_016864026.1:p.Ile927Val
XM_017008538.2:c.2779A>G	XP_016864027.1:p.Ile927Val
XM_024454179.1:c.2779A>G	XP_024309947.1:p.Ile927Val
XM_024454180.1:c.2779A>G	XP_024309948.1:p.Ile927Val
XM_024454181.1:c.1429A>G	XP_024309949.1:p.Ile477Val
XR_001741315.2:n.2971A>G