Canonical Allele Identifier: CA4892762

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139732001G>C , CM000670.2:g.139732001G>C	GRCh38
NC_000008.10:g.140744244G>C , CM000670.1:g.140744244G>C	GRCh37
NC_000008.9:g.140813426G>C	NCBI36
NG_016478.2:g.731579C>G
NG_016478.3:g.731579C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.3257C>G MANE Select	ENSP00000405060.3:p.Ser1086Cys
ENST00000648948.2:c.3257C>G	ENSP00000498020.1:p.Ser1086Cys
ENST00000389328.8:c.3551C>G	ENSP00000373979.4:p.Ser1184Cys
ENST00000438773.2:c.3257C>G	ENSP00000405060.2:p.Ser1086Cys
ENST00000519482.1:n.344C>G
ENST00000520857.5:c.2787C>G
ENST00000521667.5:n.1662C>G
ENST00000521700.5:n.303C>G
ENST00000522504.5:n.410C>G
NM_001160372.2:c.3257C>G	NP_001153844.1:p.Ser1086Cys
NM_031466.6:c.3551C>G	NP_113654.4:p.Ser1184Cys
XM_005251077.3:c.3257C>G	XP_005251134.1:p.Ser1086Cys
XM_011517326.1:c.3524C>G	XP_011515628.1:p.Ser1175Cys
XM_011517329.1:c.2645C>G	XP_011515631.1:p.Ser882Cys
XM_011517330.1:c.1706C>G	XP_011515632.1:p.Ser569Cys
NM_001160372.3:c.3257C>G	NP_001153844.1:p.Ser1086Cys
NM_001321646.1:c.3230C>G	NP_001308575.1:p.Ser1077Cys
NM_031466.7:c.3551C>G	NP_113654.4:p.Ser1184Cys
XM_011517326.2:c.3524C>G	XP_011515628.1:p.Ser1175Cys
XM_011517330.2:c.1706C>G	XP_011515632.1:p.Ser569Cys
XM_017013894.2:c.1877C>G	XP_016869383.1:p.Ser626Cys
NM_001160372.4:c.3257C>G MANE Select	NP_001153844.1:p.Ser1086Cys
NM_001321646.2:c.3230C>G	NP_001308575.1:p.Ser1077Cys
NM_001374682.1:c.3278C>G	NP_001361611.1:p.Ser1093Cys
NM_001374683.1:c.3146C>G	NP_001361612.1:p.Ser1049Cys
NM_001374684.1:c.3113C>G	NP_001361613.1:p.Ser1038Cys
NM_031466.8:c.3257C>G	NP_113654.5:p.Ser1086Cys
NR_164662.1:n.3419C>G