Canonical Allele Identifier: CA358873726

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183701696G>T , CM000666.2:g.183701696G>T	GRCh38
NC_000004.11:g.184622849G>T , CM000666.1:g.184622849G>T	GRCh37
NC_000004.10:g.184859843G>T	NCBI36
NG_033102.1:g.47430G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.2852-1G>T MANE Select	NP_068761.4:n.2852-1G>T
ENST00000334690.11:c.2852-1G>T MANE Select	ENSP00000335371.6:n.2852-1G>T
NM_021942.5:c.2852-1G>T	NP_068761.4:n.2852-1G>T
NM_199053.2:c.2852-1G>T	NP_951008.1:n.2852-1G>T
NM_199053.3:c.2852-1G>T	NP_951008.1:n.2852-1G>T
ENST00000334690.10:c.2852-1G>T	ENSP00000335371.6:n.2852-1G>T
ENST00000357207.8:c.2852-1G>T	ENSP00000349738.4:n.2852-1G>T
ENST00000505676.5:c.*966-1G>T	ENSP00000422915.1:n.*966-1G>T
ENST00000506426.1:n.37G>T
ENST00000511955.5:n.844G>T
ENST00000512476.1:c.1670-1G>T	ENSP00000421004.1:n.1670-1G>T
XM_011532180.1:c.2852-1G>T	XP_011530482.1:n.2852-1G>T
XM_017008537.2:c.2852-1G>T	XP_016864026.1:n.2852-1G>T
XM_024454179.1:c.2852-1G>T	XP_024309947.1:n.2852-1G>T
XM_024454180.1:c.2852-1G>T	XP_024309948.1:n.2852-1G>T
XM_024454181.1:c.1502-1G>T	XP_024309949.1:n.1502-1G>T
XR_001741315.2:n.3044-1G>T