Canonical Allele Identifier: CA1824410128

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139910304C= , CM000670.2:g.139910304C=	GRCh38
NC_000008.10:g.140922548C= , CM000670.1:g.140922548C=	GRCh37
NC_000008.9:g.140991730C=	NCBI36
NG_016478.2:g.553276G=
NG_016478.3:g.553276G=

Transcript Alleles

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