Canonical Allele Identifier: CA3151878

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183684162T>A , CM000666.2:g.183684162T>A	GRCh38
NC_000004.11:g.184605315T>A , CM000666.1:g.184605315T>A	GRCh37
NC_000004.10:g.184842309T>A	NCBI36
NG_033102.1:g.29896T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.1305T>A MANE Select	NP_068761.4:p.Leu435=
ENST00000334690.11:c.1305T>A MANE Select	ENSP00000335371.6:p.Leu435=
NM_021942.5:c.1305T>A	NP_068761.4:p.Leu435=
NM_199053.2:c.1305T>A	NP_951008.1:p.Leu435=
NM_199053.3:c.1305T>A	NP_951008.1:p.Leu435=
ENST00000334690.10:c.1305T>A	ENSP00000335371.6:p.Leu435=
ENST00000357207.8:c.1305T>A	ENSP00000349738.4:p.Leu435=
ENST00000505676.5:c.348+156T>A	ENSP00000422915.1:n.348+156T>A
ENST00000512476.1:c.123T>A	ENSP00000421004.1:p.Leu41=
XM_011532180.1:c.1305T>A	XP_011530482.1:p.Leu435=
XM_017008537.2:c.1305T>A	XP_016864026.1:p.Leu435=
XM_017008538.2:c.1305T>A	XP_016864027.1:p.Leu435=
XM_024454179.1:c.1305T>A	XP_024309947.1:p.Leu435=
XM_024454180.1:c.1305T>A	XP_024309948.1:p.Leu435=
XM_024454181.1:c.-46T>A	XP_024309949.1:n.-46T>A
XR_001741315.2:n.1497T>A