Canonical Allele Identifier: CA3152471

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183708410C>T , CM000666.2:g.183708410C>T	GRCh38
NC_000004.11:g.184629563C>T , CM000666.1:g.184629563C>T	GRCh37
NC_000004.10:g.184866557C>T	NCBI36
NG_033102.1:g.54144C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.3193C>T MANE Select	NP_068761.4:p.Arg1065Ter
ENST00000334690.11:c.3193C>T MANE Select	ENSP00000335371.6:p.Arg1065Ter
NM_021942.5:c.3193C>T	NP_068761.4:p.Arg1065Ter
NM_199053.2:c.3193C>T	NP_951008.1:p.Arg1065Ter
NM_199053.3:c.3193C>T	NP_951008.1:p.Arg1065Ter
ENST00000334690.10:c.3193C>T	ENSP00000335371.6:p.Arg1065Ter
ENST00000357207.8:c.3193C>T	ENSP00000349738.4:p.Arg1065Ter
ENST00000505676.5:c.*1307C>T	ENSP00000422915.1:n.*1307C>T
ENST00000511955.5:n.1186C>T
ENST00000512476.1:c.2011C>T	ENSP00000421004.1:p.Arg671Ter
XM_024454179.1:c.3193C>T	XP_024309947.1:p.Arg1065Ter
XM_024454180.1:c.3193C>T	XP_024309948.1:p.Arg1065Ter
XM_024454181.1:c.1843C>T	XP_024309949.1:p.Arg615Ter
XR_001741315.2:n.3466C>T