Canonical Allele Identifier: CA372316548

Gene: TRAPPC9

Linked Data

• MyVariant Identifiers: chr8:g.141370236C>A (hg19) ; chr8:g.140360137C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140360137C>A , CM000670.2:g.140360137C>A	GRCh38
NC_000008.10:g.141370236C>A , CM000670.1:g.141370236C>A	GRCh37
NC_000008.9:g.141439418C>A	NCBI36
NG_016478.2:g.103443G>T
NG_016478.3:g.103443G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1408G>T MANE Select	ENSP00000405060.3:p.Ala470Ser
ENST00000648948.2:c.1408G>T	ENSP00000498020.1:p.Ala470Ser
ENST00000389328.8:c.1702G>T	ENSP00000373979.4:p.Ala568Ser
ENST00000438773.2:c.1408G>T	ENSP00000405060.2:p.Ala470Ser
ENST00000520857.5:c.938G>T
NM_001160372.2:c.1408G>T	NP_001153844.1:p.Ala470Ser
NM_031466.6:c.1702G>T	NP_113654.4:p.Ala568Ser
XM_005251077.3:c.1408G>T	XP_005251134.1:p.Ala470Ser
XM_011517326.1:c.1675G>T	XP_011515628.1:p.Ala559Ser
XM_011517327.1:c.1702G>T	XP_011515629.1:p.Ala568Ser
XM_011517328.1:c.1702G>T	XP_011515630.1:p.Ala568Ser
XM_011517329.1:c.796G>T	XP_011515631.1:p.Ala266Ser
XR_928355.1:n.1717G>T
NM_001160372.3:c.1408G>T	NP_001153844.1:p.Ala470Ser
NM_001321646.1:c.1381G>T	NP_001308575.1:p.Ala461Ser
NM_031466.7:c.1702G>T	NP_113654.4:p.Ala568Ser
XM_011517326.2:c.1675G>T	XP_011515628.1:p.Ala559Ser
XM_011517328.2:c.1702G>T	XP_011515630.1:p.Ala568Ser
XM_017013893.1:c.1702G>T	XP_016869382.1:p.Ala568Ser
XM_017013894.2:c.28G>T	XP_016869383.1:p.Ala10Ser
XR_928355.2:n.1717G>T
NM_001160372.4:c.1408G>T MANE Select	NP_001153844.1:p.Ala470Ser
NM_001321646.2:c.1381G>T	NP_001308575.1:p.Ala461Ser
NM_001374682.1:c.1429G>T	NP_001361611.1:p.Ala477Ser
NM_001374683.1:c.1408G>T	NP_001361612.1:p.Ala470Ser
NM_001374684.1:c.1351+10827G>T	NP_001361613.1:n.1351+10827G>T
NM_031466.8:c.1408G>T	NP_113654.5:p.Ala470Ser
NR_164662.1:n.1497G>T