Canonical Allele Identifier: CA4893466

Gene: TRAPPC9

Linked Data

• dbSNP Id: rs774589663
• ExAC: 8:141370286 T / G
• gnomAD v2: 8-141370286-T-G
• gnomAD v3: 8-140360187-T-G
• gnomAD v4: 8-140360187-T-G
• MyVariant Identifiers: chr8:g.141370286T>G (hg19) ; chr8:g.140360187T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140360187T>G , CM000670.2:g.140360187T>G	GRCh38
NC_000008.10:g.141370286T>G , CM000670.1:g.141370286T>G	GRCh37
NC_000008.9:g.141439468T>G	NCBI36
NG_016478.2:g.103393A>C
NG_016478.3:g.103393A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.1358A>C MANE Select	ENSP00000405060.3:p.His453Pro
ENST00000648948.2:c.1358A>C	ENSP00000498020.1:p.His453Pro
ENST00000389328.8:c.1652A>C	ENSP00000373979.4:p.His551Pro
ENST00000438773.2:c.1358A>C	ENSP00000405060.2:p.His453Pro
ENST00000520857.5:c.888A>C
NM_001160372.2:c.1358A>C	NP_001153844.1:p.His453Pro
NM_031466.6:c.1652A>C	NP_113654.4:p.His551Pro
XM_005251077.3:c.1358A>C	XP_005251134.1:p.His453Pro
XM_011517326.1:c.1625A>C	XP_011515628.1:p.His542Pro
XM_011517327.1:c.1652A>C	XP_011515629.1:p.His551Pro
XM_011517328.1:c.1652A>C	XP_011515630.1:p.His551Pro
XM_011517329.1:c.746A>C	XP_011515631.1:p.His249Pro
XR_928355.1:n.1667A>C
NM_001160372.3:c.1358A>C	NP_001153844.1:p.His453Pro
NM_001321646.1:c.1331A>C	NP_001308575.1:p.His444Pro
NM_031466.7:c.1652A>C	NP_113654.4:p.His551Pro
XM_011517326.2:c.1625A>C	XP_011515628.1:p.His542Pro
XM_011517328.2:c.1652A>C	XP_011515630.1:p.His551Pro
XM_017013893.1:c.1652A>C	XP_016869382.1:p.His551Pro
XM_017013894.2:c.-23A>C	XP_016869383.1:n.-23A>C
XR_928355.2:n.1667A>C
NM_001160372.4:c.1358A>C MANE Select	NP_001153844.1:p.His453Pro
NM_001321646.2:c.1331A>C	NP_001308575.1:p.His444Pro
NM_001374682.1:c.1379A>C	NP_001361611.1:p.His460Pro
NM_001374683.1:c.1358A>C	NP_001361612.1:p.His453Pro
NM_001374684.1:c.1351+10777A>C	NP_001361613.1:n.1351+10777A>C
NM_031466.8:c.1358A>C	NP_113654.5:p.His453Pro
NR_164662.1:n.1447A>C