Canonical Allele Identifier: CA3152410
Community Standard Title: NM_021942.6(TRAPPC11):c.3014C>T (p.Pro1005Leu)
Gene: TRAPPC11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.183705029C>T , CM000666.2:g.183705029C>T GRCh38
NC_000004.11:g.184626182C>T , CM000666.1:g.184626182C>T GRCh37
NC_000004.10:g.184863176C>T NCBI36
NG_033102.1:g.50763C>T

Transcript Alleles

HGVS Amino-acid Change
NM_021942.6:c.3014C>T MANE Select NP_068761.4:p.Pro1005Leu
ENST00000334690.11:c.3014C>T MANE Select ENSP00000335371.6:p.Pro1005Leu
NM_021942.5:c.3014C>T NP_068761.4:p.Pro1005Leu
NM_199053.2:c.3014C>T NP_951008.1:p.Pro1005Leu
NM_199053.3:c.3014C>T NP_951008.1:p.Pro1005Leu
ENST00000334690.10:c.3014C>T ENSP00000335371.6:p.Pro1005Leu
ENST00000357207.8:c.3014C>T ENSP00000349738.4:p.Pro1005Leu
ENST00000505676.5:c.*1128C>T ENSP00000422915.1:n.*1128C>T
ENST00000506426.1:n.200C>T
ENST00000511955.5:n.1007C>T
ENST00000512476.1:c.1832C>T ENSP00000421004.1:p.Pro611Leu
XM_011532180.1:c.3014C>T XP_011530482.1:p.Pro1005Leu
XM_017008537.2:c.3014C>T XP_016864026.1:p.Pro1005Leu
XM_024454179.1:c.3014C>T XP_024309947.1:p.Pro1005Leu
XM_024454180.1:c.3014C>T XP_024309948.1:p.Pro1005Leu
XM_024454181.1:c.1664C>T XP_024309949.1:p.Pro555Leu
XR_001741315.2:n.3206C>T