Canonical Allele Identifier: CA372316619

Gene: TRAPPC9

Linked Data

• dbSNP Id: rs1365948642
• gnomAD v3: 8-140360169-A-G
• gnomAD v4: 8-140360169-A-G
• MyVariant Identifiers: chr8:g.141370268A>G (hg19) ; chr8:g.140360169A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140360169A>G , CM000670.2:g.140360169A>G	GRCh38
NC_000008.10:g.141370268A>G , CM000670.1:g.141370268A>G	GRCh37
NC_000008.9:g.141439450A>G	NCBI36
NG_016478.2:g.103411T>C
NG_016478.3:g.103411T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1376T>C MANE Select	ENSP00000405060.3:p.Val459Ala
ENST00000648948.2:c.1376T>C	ENSP00000498020.1:p.Val459Ala
ENST00000389328.8:c.1670T>C	ENSP00000373979.4:p.Val557Ala
ENST00000438773.2:c.1376T>C	ENSP00000405060.2:p.Val459Ala
ENST00000520857.5:c.906T>C
NM_001160372.2:c.1376T>C	NP_001153844.1:p.Val459Ala
NM_031466.6:c.1670T>C	NP_113654.4:p.Val557Ala
XM_005251077.3:c.1376T>C	XP_005251134.1:p.Val459Ala
XM_011517326.1:c.1643T>C	XP_011515628.1:p.Val548Ala
XM_011517327.1:c.1670T>C	XP_011515629.1:p.Val557Ala
XM_011517328.1:c.1670T>C	XP_011515630.1:p.Val557Ala
XM_011517329.1:c.764T>C	XP_011515631.1:p.Val255Ala
XR_928355.1:n.1685T>C
NM_001160372.3:c.1376T>C	NP_001153844.1:p.Val459Ala
NM_001321646.1:c.1349T>C	NP_001308575.1:p.Val450Ala
NM_031466.7:c.1670T>C	NP_113654.4:p.Val557Ala
XM_011517326.2:c.1643T>C	XP_011515628.1:p.Val548Ala
XM_011517328.2:c.1670T>C	XP_011515630.1:p.Val557Ala
XM_017013893.1:c.1670T>C	XP_016869382.1:p.Val557Ala
XM_017013894.2:c.-5T>C	XP_016869383.1:n.-5T>C
XR_928355.2:n.1685T>C
NM_001160372.4:c.1376T>C MANE Select	NP_001153844.1:p.Val459Ala
NM_001321646.2:c.1349T>C	NP_001308575.1:p.Val450Ala
NM_001374682.1:c.1397T>C	NP_001361611.1:p.Val466Ala
NM_001374683.1:c.1376T>C	NP_001361612.1:p.Val459Ala
NM_001374684.1:c.1351+10795T>C	NP_001361613.1:n.1351+10795T>C
NM_031466.8:c.1376T>C	NP_113654.5:p.Val459Ala
NR_164662.1:n.1465T>C