Canonical Allele Identifier: CA2536950454

Gene: TAB2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149378242_149378253del , CM000668.2:g.149378242_149378253del	GRCh38
NC_000006.11:g.149699378_149699389del , CM000668.1:g.149699378_149699389del	GRCh37
NC_000006.10:g.149741071_149741082del	NCBI36
NG_021386.1:g.64943_64954del
NG_021386.2:g.165319_165330del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703212.1:n.742_753del
ENST00000703213.1:c.327_338del	ENSP00000515239.1:p.Asp109_Gln113delinsGlu
ENST00000636456.1:c.-96-430_-96-419del	ENSP00000490379.1:n.-96-430_-96-419del
ENST00000637181.2:c.327_338del MANE Select	ENSP00000490618.1:p.Asp109_Gln113delinsGlu
ENST00000367456.5:c.327_338del	ENSP00000356426.1:p.Asp109_Gln113delinsGlu
ENST00000470466.5:c.327_338del	ENSP00000432709.1:p.Asp109_Gln113delinsGlu
ENST00000538427.5:c.327_338del	ENSP00000445752.1:p.Asp109_Gln113delinsGlu
ENST00000606202.1:c.105_116del	ENSP00000476139.1:p.Asp35_Gln39delinsGlu
NM_001292034.2:c.327_338del	NP_001278963.1:p.Asp109_Gln113delinsGlu
NM_001292035.2:c.231_242del	NP_001278964.1:p.Asp77_Gln81delinsGlu
NM_015093.5:c.327_338del	NP_055908.1:p.Asp109_Gln113delinsGlu
XM_006715403.2:c.327_338del	XP_006715466.1:p.Asp109_Gln113delinsGlu
XM_011535633.1:c.327_338del	XP_011533935.1:p.Asp109_Gln113delinsGlu
XM_011535634.1:c.327_338del	XP_011533936.1:p.Asp109_Gln113delinsGlu
XM_011535633.2:c.327_338del	XP_011533935.1:p.Asp109_Gln113delinsGlu
XM_017010591.1:c.327_338del	XP_016866080.1:p.Asp109_Gln113delinsGlu
XM_017010592.2:c.327_338del	XP_016866081.1:p.Asp109_Gln113delinsGlu
NM_001292034.3:c.327_338del MANE Select	NP_001278963.1:p.Asp109_Gln113delinsGlu
NM_001292035.3:c.231_242del	NP_001278964.1:p.Asp77_Gln81delinsGlu
NM_001369506.1:c.327_338del	NP_001356435.1:p.Asp109_Gln113delinsGlu
NM_015093.6:c.327_338del	NP_055908.1:p.Asp109_Gln113delinsGlu