Canonical Allele Identifier: CA1824410140

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139910320A= , CM000670.2:g.139910320A=	GRCh38
NC_000008.10:g.140922564A= , CM000670.1:g.140922564A=	GRCh37
NC_000008.9:g.140991746A=	NCBI36
NG_016478.2:g.553260T=
NG_016478.3:g.553260T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000438773.4:c.2811-20T= MANE Select	ENSP00000405060.3:n.2811-20T=
ENST00000648948.2:c.2811-20T=	ENSP00000498020.1:n.2811-20T=
ENST00000389328.8:c.3105-20T=	ENSP00000373979.4:n.3105-20T=
ENST00000438773.2:c.2811-20T=	ENSP00000405060.2:n.2811-20T=
ENST00000520857.5:c.2341-20T=
ENST00000521667.5:n.1216-20T=
ENST00000523777.5:n.420-20T=
ENST00000524162.5:n.237-20T=
NM_001160372.2:c.2811-20T=	NP_001153844.1:n.2811-20T=
NM_031466.6:c.3105-20T=	NP_113654.4:n.3105-20T=
XM_005251077.3:c.2811-20T=	XP_005251134.1:n.2811-20T=
XM_011517326.1:c.3078-20T=	XP_011515628.1:n.3078-20T=
XM_011517327.1:c.3105-20T=	XP_011515629.1:n.3105-20T=
XM_011517328.1:c.3105-20T=	XP_011515630.1:n.3105-20T=
XM_011517329.1:c.2199-20T=	XP_011515631.1:n.2199-20T=
XM_011517330.1:c.1260-20T=	XP_011515632.1:n.1260-20T=
XR_928355.1:n.3175-20T=
NM_001160372.3:c.2811-20T=	NP_001153844.1:n.2811-20T=
NM_001321646.1:c.2784-20T=	NP_001308575.1:n.2784-20T=
NM_031466.7:c.3105-20T=	NP_113654.4:n.3105-20T=
XM_011517326.2:c.3078-20T=	XP_011515628.1:n.3078-20T=
XM_011517328.2:c.3105-20T=	XP_011515630.1:n.3105-20T=
XM_011517330.2:c.1260-20T=	XP_011515632.1:n.1260-20T=
XM_017013894.2:c.1431-20T=	XP_016869383.1:n.1431-20T=
XR_928355.2:n.3175-20T=
NM_001160372.4:c.2811-20T= MANE Select	NP_001153844.1:n.2811-20T=
NM_001321646.2:c.2784-20T=	NP_001308575.1:n.2784-20T=
NM_001374682.1:c.2832-20T=	NP_001361611.1:n.2832-20T=
NM_001374683.1:c.2700-20T=	NP_001361612.1:n.2700-20T=
NM_001374684.1:c.2667-20T=	NP_001361613.1:n.2667-20T=
NM_031466.8:c.2811-20T=	NP_113654.5:n.2811-20T=
NR_164662.1:n.2900-20T=