Canonical Allele Identifier: CA2678147533
Gene: BTNL2 HGNC NCBI
TSBP1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32401730_32401754dup , CM000668.2:g.32401730_32401754dup GRCh38
NC_000006.11:g.32369507_32369531dup , CM000668.1:g.32369507_32369531dup GRCh37
NC_000006.10:g.32477485_32477509dup NCBI36
NG_054759.1:g.12133_12157dup

Transcript Alleles

HGVS Amino-acid change
ENST00000374993.5:n.158+38_158+62dup (BTNL2)
ENST00000454136.8:c.730+38_730+62dup (BTNL2) MANE Select ENSP00000390613.3:n.730+38_730+62dup
ENST00000465865.6:c.*5+38_*5+62dup (BTNL2) ENSP00000420063.1:n.*5+38_*5+62dup
ENST00000544175.3:c.207+38_207+62dup (BTNL2) ENSP00000443364.2:n.207+38_207+62dup
ENST00000374993.4:c.730+38_730+62dup (BTNL2) ENSP00000364132.1:n.730+38_730+62dup
ENST00000454136.7:c.730+38_730+62dup (BTNL2) ENSP00000390613.3:n.730+38_730+62dup
ENST00000465865.5:c.212+38_212+62dup (BTNL2) ENSP00000420063.1:n.212+38_212+62dup
ENST00000544175.2:c.-102+38_-102+62dup (BTNL2) ENSP00000443364.1:n.-102+38_-102+62dup
NM_001304561.1:c.730+38_730+62dup (BTNL2) NP_001291490.1:n.730+38_730+62dup
XM_011514755.1:c.730+38_730+62dup (BTNL2) XP_011513057.1:n.730+38_730+62dup
XM_011514756.1:c.448+38_448+62dup (BTNL2) XP_011513058.1:n.448+38_448+62dup
XM_011515039.1:c.482-3724_482-3700dup (TSBP1-AS1) XP_011513341.1:n.482-3724_482-3700dup
NR_136245.1:n.303-3724_303-3700dup (TSBP1-AS1)
XM_017011057.1:c.730+38_730+62dup (BTNL2) XP_016866546.1:n.730+38_730+62dup
NM_001304561.2:c.730+38_730+62dup (BTNL2) MANE Select NP_001291490.1:n.730+38_730+62dup