Canonical Allele Identifier: CA455867090

Gene: TBL2

Linked Data

• MyVariant Identifiers: chr7:g.72987266A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73572936A>T , CM000669.2:g.73572936A>T	GRCh38
NC_000007.13:g.72987266A>T , CM000669.1:g.72987266A>T	GRCh37
NC_000007.12:g.72625202A>T	NCBI36
NG_023281.1:g.10748T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000305632.11:c.633T>A MANE Select	ENSP00000307260.4:p.Thr211=
ENST00000305632.9:c.633T>A	ENSP00000307260.4:p.Thr211=
ENST00000417008.5:c.*370T>A	ENSP00000407503.1:n.*370T>A
ENST00000424598.5:c.*550T>A	ENSP00000398195.1:n.*550T>A
ENST00000426966.5:c.*566T>A	ENSP00000410737.1:n.*566T>A
ENST00000432538.5:c.525T>A	ENSP00000413979.1:p.Thr175=
ENST00000433464.5:c.*242T>A	ENSP00000404242.1:n.*242T>A
ENST00000435792.5:c.*759T>A	ENSP00000408255.1:n.*759T>A
ENST00000437521.5:c.*566T>A	ENSP00000400569.1:n.*566T>A
ENST00000450285.5:c.*79T>A	ENSP00000409820.1:n.*79T>A
ENST00000452475.5:n.718T>A
ENST00000459913.5:n.800T>A
ENST00000495885.1:n.397T>A
ENST00000610724.4:c.633T>A	ENSP00000484750.1:p.Thr211=
NM_012453.2:c.633T>A	NP_036585.1:p.Thr211=
XM_006715923.2:c.534T>A	XP_006715986.1:p.Thr178=
XM_011516026.1:c.525T>A	XP_011514328.1:p.Thr175=
XM_011516027.1:c.138T>A	XP_011514329.1:p.Thr46=
NM_001362660.1:c.534T>A	NP_001349589.1:p.Thr178=
NM_001362661.1:c.138T>A	NP_001349590.1:p.Thr46=
NM_001362662.1:c.138T>A	NP_001349591.1:p.Thr46=
NM_001362663.1:c.138T>A	NP_001349592.1:p.Thr46=
NM_012453.3:c.633T>A	NP_036585.1:p.Thr211=
XM_006715923.4:c.534T>A	XP_006715986.1:p.Thr178=
XM_024446709.1:c.534T>A	XP_024302477.1:p.Thr178=
XM_024446712.1:c.138T>A	XP_024302480.1:p.Thr46=
XR_001744627.2:n.689T>A
NM_001362660.2:c.534T>A	NP_001349589.1:p.Thr178=
NM_001362661.2:c.138T>A	NP_001349590.1:p.Thr46=
NM_001362662.2:c.138T>A	NP_001349591.1:p.Thr46=
NM_001362663.2:c.138T>A	NP_001349592.1:p.Thr46=
NM_012453.4:c.633T>A MANE Select	NP_036585.1:p.Thr211=