Canonical Allele Identifier: CA10630396

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139730957G>A , CM000670.2:g.139730957G>A	GRCh38
NC_000008.10:g.140743200G>A , CM000670.1:g.140743200G>A	GRCh37
NC_000008.9:g.140812382G>A	NCBI36
NG_016478.2:g.732623C>T
NG_016478.3:g.732623C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.*104C>T MANE Select	ENSP00000405060.3:n.*104C>T
ENST00000648948.2:c.*104C>T	ENSP00000498020.1:n.*104C>T
ENST00000389328.8:c.*104C>T	ENSP00000373979.4:n.*104C>T
ENST00000438773.2:c.*104C>T	ENSP00000405060.2:n.*104C>T
ENST00000520857.5:c.3081C>T
ENST00000521667.5:n.1956C>T
NM_001160372.2:c.*104C>T	NP_001153844.1:n.*104C>T
NM_031466.6:c.*104C>T	NP_113654.4:n.*104C>T
XM_005251077.3:c.*104C>T	XP_005251134.1:n.*104C>T
XM_011517326.1:c.*104C>T	XP_011515628.1:n.*104C>T
XM_011517329.1:c.*104C>T	XP_011515631.1:n.*104C>T
XM_011517330.1:c.*104C>T	XP_011515632.1:n.*104C>T
NM_001160372.3:c.*104C>T	NP_001153844.1:n.*104C>T
NM_001321646.1:c.*104C>T	NP_001308575.1:n.*104C>T
NM_031466.7:c.*104C>T	NP_113654.4:n.*104C>T
XM_011517326.2:c.*104C>T	XP_011515628.1:n.*104C>T
XM_011517330.2:c.*104C>T	XP_011515632.1:n.*104C>T
XM_017013894.2:c.*104C>T	XP_016869383.1:n.*104C>T
NM_001160372.4:c.*104C>T MANE Select	NP_001153844.1:n.*104C>T
NM_001321646.2:c.*104C>T	NP_001308575.1:n.*104C>T
NM_001374682.1:c.*104C>T	NP_001361611.1:n.*104C>T
NM_001374683.1:c.*104C>T	NP_001361612.1:n.*104C>T
NM_001374684.1:c.*104C>T	NP_001361613.1:n.*104C>T
NM_031466.8:c.*104C>T	NP_113654.5:n.*104C>T
NR_164662.1:n.3713C>T