Canonical Allele Identifier: CA209254

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.140439194A>G , CM000670.2:g.140439194A>G	GRCh38
NC_000008.10:g.141449293A>G , CM000670.1:g.141449293A>G	GRCh37
NC_000008.9:g.141518475A>G	NCBI36
NG_016478.2:g.24386T>C
NG_016478.3:g.24386T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.588T>C MANE Select	ENSP00000405060.3:p.His196=
ENST00000648948.2:c.588T>C	ENSP00000498020.1:p.His196=
ENST00000389328.8:c.882T>C	ENSP00000373979.4:p.His294=
ENST00000438773.2:c.588T>C	ENSP00000405060.2:p.His196=
ENST00000520857.5:c.145T>C
NM_001160372.2:c.588T>C	NP_001153844.1:p.His196=
NM_031466.6:c.882T>C	NP_113654.4:p.His294=
XM_005251077.3:c.588T>C	XP_005251134.1:p.His196=
XM_011517326.1:c.882T>C	XP_011515628.1:p.His294=
XM_011517327.1:c.882T>C	XP_011515629.1:p.His294=
XM_011517328.1:c.882T>C	XP_011515630.1:p.His294=
XM_011517329.1:c.-25T>C	XP_011515631.1:n.-25T>C
XR_928355.1:n.897T>C
NM_001160372.3:c.588T>C	NP_001153844.1:p.His196=
NM_001321646.1:c.588T>C	NP_001308575.1:p.His196=
NM_031466.7:c.882T>C	NP_113654.4:p.His294=
XM_011517326.2:c.882T>C	XP_011515628.1:p.His294=
XM_011517328.2:c.882T>C	XP_011515630.1:p.His294=
XM_017013893.1:c.882T>C	XP_016869382.1:p.His294=
XR_928355.2:n.897T>C
NM_001160372.4:c.588T>C MANE Select	NP_001153844.1:p.His196=
NM_001321646.2:c.588T>C	NP_001308575.1:p.His196=
NM_001374682.1:c.609T>C	NP_001361611.1:p.His203=
NM_001374683.1:c.588T>C	NP_001361612.1:p.His196=
NM_001374684.1:c.588T>C	NP_001361613.1:p.His196=
NM_031466.8:c.588T>C	NP_113654.5:p.His196=
NR_164662.1:n.704T>C