Canonical Allele Identifier: CA4041349
Gene: TAB2 HGNC NCBI

Linked Data

dbSNP Id: rs759531579

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149377997_149378000del , CM000668.2:g.149377997_149378000del GRCh38
NC_000006.11:g.149699133_149699136del , CM000668.1:g.149699133_149699136del GRCh37
NC_000006.10:g.149740826_149740829del NCBI36
NG_021386.1:g.64698_64701del
NG_021386.2:g.165074_165077del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703212.1:n.518-21_518-18del
ENST00000703213.1:c.103-21_103-18del ENSP00000515239.1:n.103-21_103-18del
ENST00000636456.1:c.-96-675_-96-672del ENSP00000490379.1:n.-96-675_-96-672del
ENST00000637181.2:c.103-21_103-18del MANE Select ENSP00000490618.1:n.103-21_103-18del
ENST00000367456.5:c.103-21_103-18del ENSP00000356426.1:n.103-21_103-18del
ENST00000470466.5:c.103-21_103-18del ENSP00000432709.1:n.103-21_103-18del
ENST00000538427.5:c.103-21_103-18del ENSP00000445752.1:n.103-21_103-18del
ENST00000606202.1:c.-120-21_-120-18del ENSP00000476139.1:n.-120-21_-120-18del
NM_001292034.2:c.103-21_103-18del NP_001278963.1:n.103-21_103-18del
NM_001292035.2:c.7-21_7-18del NP_001278964.1:n.7-21_7-18del
NM_015093.5:c.103-21_103-18del NP_055908.1:n.103-21_103-18del
XM_006715403.2:c.103-21_103-18del XP_006715466.1:n.103-21_103-18del
XM_011535633.1:c.103-21_103-18del XP_011533935.1:n.103-21_103-18del
XM_011535634.1:c.103-21_103-18del XP_011533936.1:n.103-21_103-18del
XM_011535633.2:c.103-21_103-18del XP_011533935.1:n.103-21_103-18del
XM_017010591.1:c.103-21_103-18del XP_016866080.1:n.103-21_103-18del
XM_017010592.2:c.103-21_103-18del XP_016866081.1:n.103-21_103-18del
NM_001292034.3:c.103-21_103-18del MANE Select NP_001278963.1:n.103-21_103-18del
NM_001292035.3:c.7-21_7-18del NP_001278964.1:n.7-21_7-18del
NM_001369506.1:c.103-21_103-18del NP_001356435.1:n.103-21_103-18del
NM_015093.6:c.103-21_103-18del NP_055908.1:n.103-21_103-18del