Canonical Allele Identifier: CA155806

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140450960G>A , CM000670.2:g.140450960G>A	GRCh38
NC_000008.10:g.141461059G>A , CM000670.1:g.141461059G>A	GRCh37
NC_000008.9:g.141530241G>A	NCBI36
NG_016478.2:g.12620C>T
NG_016478.3:g.12620C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.414C>T MANE Select	ENSP00000405060.3:p.Tyr138=
ENST00000648948.2:c.414C>T	ENSP00000498020.1:p.Tyr138=
ENST00000389328.8:c.708C>T	ENSP00000373979.4:p.Tyr236=
ENST00000438773.2:c.414C>T	ENSP00000405060.2:p.Tyr138=
NM_001160372.2:c.414C>T	NP_001153844.1:p.Tyr138=
NM_031466.6:c.708C>T	NP_113654.4:p.Tyr236=
XM_005251077.3:c.414C>T	XP_005251134.1:p.Tyr138=
XM_011517326.1:c.708C>T	XP_011515628.1:p.Tyr236=
XM_011517327.1:c.708C>T	XP_011515629.1:p.Tyr236=
XM_011517328.1:c.708C>T	XP_011515630.1:p.Tyr236=
XR_928355.1:n.723C>T
NM_001160372.3:c.414C>T	NP_001153844.1:p.Tyr138=
NM_001321646.1:c.414C>T	NP_001308575.1:p.Tyr138=
NM_031466.7:c.708C>T	NP_113654.4:p.Tyr236=
XM_011517326.2:c.708C>T	XP_011515628.1:p.Tyr236=
XM_011517328.2:c.708C>T	XP_011515630.1:p.Tyr236=
XM_017013893.1:c.708C>T	XP_016869382.1:p.Tyr236=
XR_928355.2:n.723C>T
NM_001160372.4:c.414C>T MANE Select	NP_001153844.1:p.Tyr138=
NM_001321646.2:c.414C>T	NP_001308575.1:p.Tyr138=
NM_001374682.1:c.414C>T	NP_001361611.1:p.Tyr138=
NM_001374683.1:c.414C>T	NP_001361612.1:p.Tyr138=
NM_001374684.1:c.414C>T	NP_001361613.1:p.Tyr138=
NM_031466.8:c.414C>T	NP_113654.5:p.Tyr138=
NR_164662.1:n.530C>T