Canonical Allele Identifier: CA149935771

Gene: TAB2

Linked Data

• dbSNP Id: rs370573714
• gnomAD v3: 6-149399954-AGTT-A
• gnomAD v4: 6-149399954-AGTT-A
• MyVariant Identifiers: chr6:g.149721091_149721093del (hg19) ; chr6:g.149399955_149399957del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149399958_149399960del , CM000668.2:g.149399958_149399960del	GRCh38
NC_000006.11:g.149721094_149721096del , CM000668.1:g.149721094_149721096del	GRCh37
NC_000006.10:g.149762787_149762789del	NCBI36
NG_012301.1:g.4600_4602del
NG_021386.1:g.86659_86661del
NG_021386.2:g.187035_187037del

Transcript Alleles

HGVS	Amino-acid change
ENST00000636456.1:c.1087+774_1087+776del	ENSP00000490379.1:n.1087+774_1087+776del
ENST00000637181.2:c.1939+774_1939+776del MANE Select	ENSP00000490618.1:n.1939+774_1939+776del
ENST00000367456.5:c.1939+774_1939+776del	ENSP00000356426.1:n.1939+774_1939+776del
ENST00000470466.5:c.*538+774_*538+776del	ENSP00000432709.1:n.*538+774_*538+776del
ENST00000484505.1:n.452+774_452+776del
ENST00000538427.5:c.1939+774_1939+776del	ENSP00000445752.1:n.1939+774_1939+776del
NM_001292034.2:c.1939+774_1939+776del	NP_001278963.1:n.1939+774_1939+776del
NM_001292035.2:c.1843+774_1843+776del	NP_001278964.1:n.1843+774_1843+776del
NM_015093.5:c.1939+774_1939+776del	NP_055908.1:n.1939+774_1939+776del
XM_006715403.2:c.1939+774_1939+776del	XP_006715466.1:n.1939+774_1939+776del
XM_011535633.1:c.1939+774_1939+776del	XP_011533935.1:n.1939+774_1939+776del
XM_011535634.1:c.1939+774_1939+776del	XP_011533936.1:n.1939+774_1939+776del
XM_011535633.2:c.1939+774_1939+776del	XP_011533935.1:n.1939+774_1939+776del
XM_017010591.1:c.1939+774_1939+776del	XP_016866080.1:n.1939+774_1939+776del
XM_017010592.2:c.1939+774_1939+776del	XP_016866081.1:n.1939+774_1939+776del
NM_001292034.3:c.1939+774_1939+776del MANE Select	NP_001278963.1:n.1939+774_1939+776del
NM_001292035.3:c.1843+774_1843+776del	NP_001278964.1:n.1843+774_1843+776del
NM_001369506.1:c.1939+774_1939+776del	NP_001356435.1:n.1939+774_1939+776del
NM_015093.6:c.1939+774_1939+776del	NP_055908.1:n.1939+774_1939+776del