Canonical Allele Identifier: CA2695207153

Gene: TAB2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149379226_149379227del , CM000668.2:g.149379226_149379227del	GRCh38
NC_000006.11:g.149700362_149700363del , CM000668.1:g.149700362_149700363del	GRCh37
NC_000006.10:g.149742055_149742056del	NCBI36
NG_021386.1:g.65927_65928del
NG_021386.2:g.166303_166304del

Transcript Alleles

HGVS	Amino-acid change
ENST00000703212.1:n.1726_1727del
ENST00000703213.1:c.1311_1312del	ENSP00000515239.1:p.Pro438GlnfsTer8
ENST00000636456.1:c.459_460del	ENSP00000490379.1:p.Pro154GlnfsTer8
ENST00000637181.2:c.1311_1312del MANE Select	ENSP00000490618.1:p.Pro438GlnfsTer8
ENST00000367456.5:c.1311_1312del	ENSP00000356426.1:p.Pro438GlnfsTer8
ENST00000470466.5:c.1311_1312del	ENSP00000432709.1:p.Pro438GlnfsTer8
ENST00000538427.5:c.1311_1312del	ENSP00000445752.1:p.Pro438GlnfsTer8
NM_001292034.2:c.1311_1312del	NP_001278963.1:p.Pro438GlnfsTer8
NM_001292035.2:c.1215_1216del	NP_001278964.1:p.Pro406GlnfsTer8
NM_015093.5:c.1311_1312del	NP_055908.1:p.Pro438GlnfsTer8
XM_006715403.2:c.1311_1312del	XP_006715466.1:p.Pro438GlnfsTer8
XM_011535633.1:c.1311_1312del	XP_011533935.1:p.Pro438GlnfsTer8
XM_011535634.1:c.1311_1312del	XP_011533936.1:p.Pro438GlnfsTer8
XM_011535633.2:c.1311_1312del	XP_011533935.1:p.Pro438GlnfsTer8
XM_017010591.1:c.1311_1312del	XP_016866080.1:p.Pro438GlnfsTer8
XM_017010592.2:c.1311_1312del	XP_016866081.1:p.Pro438GlnfsTer8
NM_001292034.3:c.1311_1312del MANE Select	NP_001278963.1:p.Pro438GlnfsTer8
NM_001292035.3:c.1215_1216del	NP_001278964.1:p.Pro406GlnfsTer8
NM_001369506.1:c.1311_1312del	NP_001356435.1:p.Pro438GlnfsTer8
NM_015093.6:c.1311_1312del	NP_055908.1:p.Pro438GlnfsTer8