Canonical Allele Identifier: CA3151848
Community Standard Title: NM_021942.6(TRAPPC11):c.1208-4G>A
Gene: TRAPPC11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.183683971G>A , CM000666.2:g.183683971G>A GRCh38
NC_000004.11:g.184605124G>A , CM000666.1:g.184605124G>A GRCh37
NC_000004.10:g.184842118G>A NCBI36
NG_033102.1:g.29705G>A

Transcript Alleles

HGVS Amino-acid Change
NM_021942.6:c.1208-4G>A MANE Select NP_068761.4:n.1208-4G>A
ENST00000334690.11:c.1208-4G>A MANE Select ENSP00000335371.6:n.1208-4G>A
NM_021942.5:c.1208-4G>A NP_068761.4:n.1208-4G>A
NM_199053.2:c.1208-4G>A NP_951008.1:n.1208-4G>A
NM_199053.3:c.1208-4G>A NP_951008.1:n.1208-4G>A
ENST00000334690.10:c.1208-4G>A ENSP00000335371.6:n.1208-4G>A
ENST00000357207.8:c.1208-4G>A ENSP00000349738.4:n.1208-4G>A
ENST00000505676.5:c.317-4G>A ENSP00000422915.1:n.317-4G>A
ENST00000512476.1:c.22G>A ENSP00000421004.1:p.Ala8Thr
XM_011532180.1:c.1208-4G>A XP_011530482.1:n.1208-4G>A
XM_017008537.2:c.1208-4G>A XP_016864026.1:n.1208-4G>A
XM_017008538.2:c.1208-4G>A XP_016864027.1:n.1208-4G>A
XM_024454179.1:c.1208-4G>A XP_024309947.1:n.1208-4G>A
XM_024454180.1:c.1208-4G>A XP_024309948.1:n.1208-4G>A
XM_024454181.1:c.-143-4G>A XP_024309949.1:n.-143-4G>A
XR_001741315.2:n.1400-4G>A