Canonical Allele Identifier: CA2678147517

Gene: BTNL2 TSBP1-AS1

Linked Data

• gnomAD v4: 6-32401711-GTGGTAGCTCCCCTCCCTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32401714_32401731del , CM000668.2:g.32401714_32401731del	GRCh38
NC_000006.11:g.32369491_32369508del , CM000668.1:g.32369491_32369508del	GRCh37
NC_000006.10:g.32477469_32477486del	NCBI36
NG_054759.1:g.12151_12168del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374993.5:n.158+56_158+73del (BTNL2)
ENST00000454136.8:c.730+56_730+73del (BTNL2) MANE Select	ENSP00000390613.3:n.730+56_730+73del
ENST00000465865.6:c.*5+56_*5+73del (BTNL2)	ENSP00000420063.1:n.*5+56_*5+73del
ENST00000544175.3:c.207+56_207+73del (BTNL2)	ENSP00000443364.2:n.207+56_207+73del
ENST00000374993.4:c.730+56_730+73del (BTNL2)	ENSP00000364132.1:n.730+56_730+73del
ENST00000454136.7:c.730+56_730+73del (BTNL2)	ENSP00000390613.3:n.730+56_730+73del
ENST00000465865.5:c.212+56_212+73del (BTNL2)	ENSP00000420063.1:n.212+56_212+73del
ENST00000544175.2:c.-102+56_-102+73del (BTNL2)	ENSP00000443364.1:n.-102+56_-102+73del
NM_001304561.1:c.730+56_730+73del (BTNL2)	NP_001291490.1:n.730+56_730+73del
XM_011514755.1:c.730+56_730+73del (BTNL2)	XP_011513057.1:n.730+56_730+73del
XM_011514756.1:c.448+56_448+73del (BTNL2)	XP_011513058.1:n.448+56_448+73del
XM_011515039.1:c.482-3740_482-3723del (TSBP1-AS1)	XP_011513341.1:n.482-3740_482-3723del
NR_136245.1:n.303-3740_303-3723del (TSBP1-AS1)
XM_017011057.1:c.730+56_730+73del (BTNL2)	XP_016866546.1:n.730+56_730+73del
NM_001304561.2:c.730+56_730+73del (BTNL2) MANE Select	NP_001291490.1:n.730+56_730+73del