Canonical Allele Identifier: CA358863689

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183680269T>G , CM000666.2:g.183680269T>G	GRCh38
NC_000004.11:g.184601422T>G , CM000666.1:g.184601422T>G	GRCh37
NC_000004.10:g.184838416T>G	NCBI36
NG_033102.1:g.26003T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.1113+2T>G MANE Select	NP_068761.4:n.1113+2T>G
ENST00000334690.11:c.1113+2T>G MANE Select	ENSP00000335371.6:n.1113+2T>G
NM_021942.5:c.1113+2T>G	NP_068761.4:n.1113+2T>G
NM_199053.2:c.1113+2T>G	NP_951008.1:n.1113+2T>G
NM_199053.3:c.1113+2T>G	NP_951008.1:n.1113+2T>G
ENST00000334690.10:c.1113+2T>G	ENSP00000335371.6:n.1113+2T>G
ENST00000357207.8:c.1113+2T>G	ENSP00000349738.4:n.1113+2T>G
ENST00000505676.5:c.222+2T>G	ENSP00000422915.1:n.222+2T>G
XM_011532180.1:c.1113+2T>G	XP_011530482.1:n.1113+2T>G
XM_017008537.2:c.1113+2T>G	XP_016864026.1:n.1113+2T>G
XM_017008538.2:c.1113+2T>G	XP_016864027.1:n.1113+2T>G
XM_024454179.1:c.1113+2T>G	XP_024309947.1:n.1113+2T>G
XM_024454180.1:c.1113+2T>G	XP_024309948.1:n.1113+2T>G
XM_024454181.1:c.-144+2T>G	XP_024309949.1:n.-144+2T>G
XR_001741315.2:n.1305+2T>G