Canonical Allele Identifier: CA15538293

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140300185A>G , CM000670.2:g.140300185A>G	GRCh38
NC_000008.10:g.141310284A>G , CM000670.1:g.141310284A>G	GRCh37
NC_000008.9:g.141379466A>G	NCBI36
NG_016478.2:g.163395T>C
NG_016478.3:g.163395T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1768+284T>C MANE Select	ENSP00000405060.3:n.1768+284T>C
ENST00000648948.2:c.1768+284T>C	ENSP00000498020.1:n.1768+284T>C
ENST00000389328.8:c.2062+284T>C	ENSP00000373979.4:n.2062+284T>C
ENST00000438773.2:c.1768+284T>C	ENSP00000405060.2:n.1768+284T>C
ENST00000520857.5:c.1298+284T>C
ENST00000521167.1:n.297+284T>C
NM_001160372.2:c.1768+284T>C	NP_001153844.1:n.1768+284T>C
NM_031466.6:c.2062+284T>C	NP_113654.4:n.2062+284T>C
XM_005251077.3:c.1768+284T>C	XP_005251134.1:n.1768+284T>C
XM_011517326.1:c.2035+284T>C	XP_011515628.1:n.2035+284T>C
XM_011517327.1:c.2062+284T>C	XP_011515629.1:n.2062+284T>C
XM_011517328.1:c.2062+284T>C	XP_011515630.1:n.2062+284T>C
XM_011517329.1:c.1156+284T>C	XP_011515631.1:n.1156+284T>C
XM_011517330.1:c.217+284T>C	XP_011515632.1:n.217+284T>C
XR_928355.1:n.2077+284T>C
NM_001160372.3:c.1768+284T>C	NP_001153844.1:n.1768+284T>C
NM_001321646.1:c.1741+284T>C	NP_001308575.1:n.1741+284T>C
NM_031466.7:c.2062+284T>C	NP_113654.4:n.2062+284T>C
XM_011517326.2:c.2035+284T>C	XP_011515628.1:n.2035+284T>C
XM_011517328.2:c.2062+284T>C	XP_011515630.1:n.2062+284T>C
XM_011517330.2:c.217+284T>C	XP_011515632.1:n.217+284T>C
XM_017013893.1:c.2062+284T>C	XP_016869382.1:n.2062+284T>C
XM_017013894.2:c.388+284T>C	XP_016869383.1:n.388+284T>C
XR_928355.2:n.2077+284T>C
NM_001160372.4:c.1768+284T>C MANE Select	NP_001153844.1:n.1768+284T>C
NM_001321646.2:c.1741+284T>C	NP_001308575.1:n.1741+284T>C
NM_001374682.1:c.1789+284T>C	NP_001361611.1:n.1789+284T>C
NM_001374683.1:c.1768+284T>C	NP_001361612.1:n.1768+284T>C
NM_001374684.1:c.1624+284T>C	NP_001361613.1:n.1624+284T>C
NM_031466.8:c.1768+284T>C	NP_113654.5:n.1768+284T>C
NR_164662.1:n.1857+284T>C