Canonical Allele Identifier: CA1619542510

Gene: BTNL2 TSBP1-AS1

Linked Data

• dbSNP Id: rs1776786678

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32401560_32401579del , CM000668.2:g.32401560_32401579del	GRCh38
NC_000006.11:g.32369337_32369356del , CM000668.1:g.32369337_32369356del	GRCh37
NC_000006.10:g.32477315_32477334del	NCBI36
NG_054759.1:g.12302_12321del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374993.5:n.158+207_158+226del (BTNL2)
ENST00000454136.8:c.730+207_730+226del (BTNL2) MANE Select	ENSP00000390613.3:n.730+207_730+226del
ENST00000465865.6:c.*5+207_*5+226del (BTNL2)	ENSP00000420063.1:n.*5+207_*5+226del
ENST00000544175.3:c.207+207_207+226del (BTNL2)	ENSP00000443364.2:n.207+207_207+226del
ENST00000374993.4:c.730+207_730+226del (BTNL2)	ENSP00000364132.1:n.730+207_730+226del
ENST00000454136.7:c.730+207_730+226del (BTNL2)	ENSP00000390613.3:n.730+207_730+226del
ENST00000465865.5:c.212+207_212+226del (BTNL2)	ENSP00000420063.1:n.212+207_212+226del
ENST00000544175.2:c.-102+207_-102+226del (BTNL2)	ENSP00000443364.1:n.-102+207_-102+226del
NM_001304561.1:c.730+207_730+226del (BTNL2)	NP_001291490.1:n.730+207_730+226del
XM_011514755.1:c.730+207_730+226del (BTNL2)	XP_011513057.1:n.730+207_730+226del
XM_011514756.1:c.448+207_448+226del (BTNL2)	XP_011513058.1:n.448+207_448+226del
XM_011515039.1:c.482-3894_482-3875del (TSBP1-AS1)	XP_011513341.1:n.482-3894_482-3875del
NR_136245.1:n.303-3894_303-3875del (TSBP1-AS1)
XM_017011057.1:c.730+207_730+226del (BTNL2)	XP_016866546.1:n.730+207_730+226del
NM_001304561.2:c.730+207_730+226del (BTNL2) MANE Select	NP_001291490.1:n.730+207_730+226del