Canonical Allele Identifier: CA206454

Gene: TRAPPC9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139885922G>A , CM000670.2:g.139885922G>A	GRCh38
NC_000008.10:g.140898166G>A , CM000670.1:g.140898166G>A	GRCh37
NC_000008.9:g.140967348G>A	NCBI36
NG_016478.2:g.577658C>T
NG_016478.3:g.577658C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438773.4:c.3012C>T MANE Select	ENSP00000405060.3:p.Asn1004=
ENST00000648948.2:c.3012C>T	ENSP00000498020.1:p.Asn1004=
ENST00000389328.8:c.3306C>T	ENSP00000373979.4:p.Asn1102=
ENST00000438773.2:c.3012C>T	ENSP00000405060.2:p.Asn1004=
ENST00000519482.1:n.142+22695C>T
ENST00000520857.5:c.2542C>T
ENST00000521667.5:n.1417C>T
ENST00000523777.5:n.621C>T
ENST00000524162.5:n.438C>T
NM_001160372.2:c.3012C>T	NP_001153844.1:p.Asn1004=
NM_031466.6:c.3306C>T	NP_113654.4:p.Asn1102=
XM_005251077.3:c.3012C>T	XP_005251134.1:p.Asn1004=
XM_011517326.1:c.3279C>T	XP_011515628.1:p.Asn1093=
XM_011517327.1:c.3306C>T	XP_011515629.1:p.Asn1102=
XM_011517328.1:c.3306C>T	XP_011515630.1:p.Asn1102=
XM_011517329.1:c.2400C>T	XP_011515631.1:p.Asn800=
XM_011517330.1:c.1461C>T	XP_011515632.1:p.Asn487=
NM_001160372.3:c.3012C>T	NP_001153844.1:p.Asn1004=
NM_001321646.1:c.2985C>T	NP_001308575.1:p.Asn995=
NM_031466.7:c.3306C>T	NP_113654.4:p.Asn1102=
XM_011517326.2:c.3279C>T	XP_011515628.1:p.Asn1093=
XM_011517328.2:c.3306C>T	XP_011515630.1:p.Asn1102=
XM_011517330.2:c.1461C>T	XP_011515632.1:p.Asn487=
XM_017013894.2:c.1632C>T	XP_016869383.1:p.Asn544=
XR_928355.2:n.3376C>T
NM_001160372.4:c.3012C>T MANE Select	NP_001153844.1:p.Asn1004=
NM_001321646.2:c.2985C>T	NP_001308575.1:p.Asn995=
NM_001374682.1:c.3033C>T	NP_001361611.1:p.Asn1011=
NM_001374683.1:c.2901C>T	NP_001361612.1:p.Asn967=
NM_001374684.1:c.2868C>T	NP_001361613.1:p.Asn956=
NM_031466.8:c.3012C>T	NP_113654.5:p.Asn1004=
NR_164662.1:n.3101C>T