Canonical Allele Identifier: CA1671914570
Gene: TAB2 HGNC NCBI

Linked Data

dbSNP Id: rs1781460249

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149377985_149377987del , CM000668.2:g.149377985_149377987del GRCh38
NC_000006.11:g.149699121_149699123del , CM000668.1:g.149699121_149699123del GRCh37
NC_000006.10:g.149740814_149740816del NCBI36
NG_021386.1:g.64686_64688del
NG_021386.2:g.165062_165064del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703212.1:n.518-33_518-31del
ENST00000703213.1:c.103-33_103-31del ENSP00000515239.1:n.103-33_103-31del
ENST00000636456.1:c.-96-687_-96-685del ENSP00000490379.1:n.-96-687_-96-685del
ENST00000637181.2:c.103-33_103-31del MANE Select ENSP00000490618.1:n.103-33_103-31del
ENST00000367456.5:c.103-33_103-31del ENSP00000356426.1:n.103-33_103-31del
ENST00000470466.5:c.103-33_103-31del ENSP00000432709.1:n.103-33_103-31del
ENST00000538427.5:c.103-33_103-31del ENSP00000445752.1:n.103-33_103-31del
ENST00000606202.1:c.-120-33_-120-31del ENSP00000476139.1:n.-120-33_-120-31del
NM_001292034.2:c.103-33_103-31del NP_001278963.1:n.103-33_103-31del
NM_001292035.2:c.7-33_7-31del NP_001278964.1:n.7-33_7-31del
NM_015093.5:c.103-33_103-31del NP_055908.1:n.103-33_103-31del
XM_006715403.2:c.103-33_103-31del XP_006715466.1:n.103-33_103-31del
XM_011535633.1:c.103-33_103-31del XP_011533935.1:n.103-33_103-31del
XM_011535634.1:c.103-33_103-31del XP_011533936.1:n.103-33_103-31del
XM_011535633.2:c.103-33_103-31del XP_011533935.1:n.103-33_103-31del
XM_017010591.1:c.103-33_103-31del XP_016866080.1:n.103-33_103-31del
XM_017010592.2:c.103-33_103-31del XP_016866081.1:n.103-33_103-31del
NM_001292034.3:c.103-33_103-31del MANE Select NP_001278963.1:n.103-33_103-31del
NM_001292035.3:c.7-33_7-31del NP_001278964.1:n.7-33_7-31del
NM_001369506.1:c.103-33_103-31del NP_001356435.1:n.103-33_103-31del
NM_015093.6:c.103-33_103-31del NP_055908.1:n.103-33_103-31del