Canonical Allele Identifier: CA372316645

Gene: TRAPPC9

Linked Data

• dbSNP Id: rs768846074
• MyVariant Identifiers: chr8:g.141370281C>G (hg19) ; chr8:g.140360182C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140360182C>G , CM000670.2:g.140360182C>G	GRCh38
NC_000008.10:g.141370281C>G , CM000670.1:g.141370281C>G	GRCh37
NC_000008.9:g.141439463C>G	NCBI36
NG_016478.2:g.103398G>C
NG_016478.3:g.103398G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1363G>C MANE Select	ENSP00000405060.3:p.Gly455Arg
ENST00000648948.2:c.1363G>C	ENSP00000498020.1:p.Gly455Arg
ENST00000389328.8:c.1657G>C	ENSP00000373979.4:p.Gly553Arg
ENST00000438773.2:c.1363G>C	ENSP00000405060.2:p.Gly455Arg
ENST00000520857.5:c.893G>C
NM_001160372.2:c.1363G>C	NP_001153844.1:p.Gly455Arg
NM_031466.6:c.1657G>C	NP_113654.4:p.Gly553Arg
XM_005251077.3:c.1363G>C	XP_005251134.1:p.Gly455Arg
XM_011517326.1:c.1630G>C	XP_011515628.1:p.Gly544Arg
XM_011517327.1:c.1657G>C	XP_011515629.1:p.Gly553Arg
XM_011517328.1:c.1657G>C	XP_011515630.1:p.Gly553Arg
XM_011517329.1:c.751G>C	XP_011515631.1:p.Gly251Arg
XR_928355.1:n.1672G>C
NM_001160372.3:c.1363G>C	NP_001153844.1:p.Gly455Arg
NM_001321646.1:c.1336G>C	NP_001308575.1:p.Gly446Arg
NM_031466.7:c.1657G>C	NP_113654.4:p.Gly553Arg
XM_011517326.2:c.1630G>C	XP_011515628.1:p.Gly544Arg
XM_011517328.2:c.1657G>C	XP_011515630.1:p.Gly553Arg
XM_017013893.1:c.1657G>C	XP_016869382.1:p.Gly553Arg
XM_017013894.2:c.-18G>C	XP_016869383.1:n.-18G>C
XR_928355.2:n.1672G>C
NM_001160372.4:c.1363G>C MANE Select	NP_001153844.1:p.Gly455Arg
NM_001321646.2:c.1336G>C	NP_001308575.1:p.Gly446Arg
NM_001374682.1:c.1384G>C	NP_001361611.1:p.Gly462Arg
NM_001374683.1:c.1363G>C	NP_001361612.1:p.Gly455Arg
NM_001374684.1:c.1351+10782G>C	NP_001361613.1:n.1351+10782G>C
NM_031466.8:c.1363G>C	NP_113654.5:p.Gly455Arg
NR_164662.1:n.1452G>C