Canonical Allele Identifier: CA1824603582

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140360168G= , CM000670.2:g.140360168G=	GRCh38
NC_000008.10:g.141370267G= , CM000670.1:g.141370267G=	GRCh37
NC_000008.9:g.141439449G=	NCBI36
NG_016478.2:g.103412C=
NG_016478.3:g.103412C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1377C= MANE Select	ENSP00000405060.3:p.Val459=
ENST00000648948.2:c.1377C=	ENSP00000498020.1:p.Val459=
ENST00000389328.8:c.1671C=	ENSP00000373979.4:p.Val557=
ENST00000438773.2:c.1377C=	ENSP00000405060.2:p.Val459=
ENST00000520857.5:c.907C=
NM_001160372.2:c.1377C=	NP_001153844.1:p.Val459=
NM_031466.6:c.1671C=	NP_113654.4:p.Val557=
XM_005251077.3:c.1377C=	XP_005251134.1:p.Val459=
XM_011517326.1:c.1644C=	XP_011515628.1:p.Val548=
XM_011517327.1:c.1671C=	XP_011515629.1:p.Val557=
XM_011517328.1:c.1671C=	XP_011515630.1:p.Val557=
XM_011517329.1:c.765C=	XP_011515631.1:p.Val255=
XR_928355.1:n.1686C=
NM_001160372.3:c.1377C=	NP_001153844.1:p.Val459=
NM_001321646.1:c.1350C=	NP_001308575.1:p.Val450=
NM_031466.7:c.1671C=	NP_113654.4:p.Val557=
XM_011517326.2:c.1644C=	XP_011515628.1:p.Val548=
XM_011517328.2:c.1671C=	XP_011515630.1:p.Val557=
XM_017013893.1:c.1671C=	XP_016869382.1:p.Val557=
XM_017013894.2:c.-4C=	XP_016869383.1:n.-4C=
XR_928355.2:n.1686C=
NM_001160372.4:c.1377C= MANE Select	NP_001153844.1:p.Val459=
NM_001321646.2:c.1350C=	NP_001308575.1:p.Val450=
NM_001374682.1:c.1398C=	NP_001361611.1:p.Val466=
NM_001374683.1:c.1377C=	NP_001361612.1:p.Val459=
NM_001374684.1:c.1351+10796C=	NP_001361613.1:n.1351+10796C=
NM_031466.8:c.1377C=	NP_113654.5:p.Val459=
NR_164662.1:n.1466C=