Canonical Allele Identifier: CA3152119

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183693079C>G , CM000666.2:g.183693079C>G	GRCh38
NC_000004.11:g.184614232C>G , CM000666.1:g.184614232C>G	GRCh37
NC_000004.10:g.184851226C>G	NCBI36
NG_033102.1:g.38813C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.2169C>G MANE Select	NP_068761.4:p.Phe723Leu
ENST00000334690.11:c.2169C>G MANE Select	ENSP00000335371.6:p.Phe723Leu
NM_021942.5:c.2169C>G	NP_068761.4:p.Phe723Leu
NM_199053.2:c.2169C>G	NP_951008.1:p.Phe723Leu
NM_199053.3:c.2169C>G	NP_951008.1:p.Phe723Leu
ENST00000334690.10:c.2169C>G	ENSP00000335371.6:p.Phe723Leu
ENST00000357207.8:c.2169C>G	ENSP00000349738.4:p.Phe723Leu
ENST00000505676.5:c.*283C>G	ENSP00000422915.1:n.*283C>G
ENST00000512476.1:c.987C>G	ENSP00000421004.1:p.Phe329Leu
XM_011532180.1:c.2169C>G	XP_011530482.1:p.Phe723Leu
XM_017008537.2:c.2169C>G	XP_016864026.1:p.Phe723Leu
XM_017008538.2:c.2169C>G	XP_016864027.1:p.Phe723Leu
XM_024454179.1:c.2169C>G	XP_024309947.1:p.Phe723Leu
XM_024454180.1:c.2169C>G	XP_024309948.1:p.Phe723Leu
XM_024454181.1:c.819C>G	XP_024309949.1:p.Phe273Leu
XR_001741315.2:n.2361C>G