Canonical Allele Identifier: CA2678148428
Gene: BTNL2 HGNC NCBI
TSBP1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32405343_32405366del , CM000668.2:g.32405343_32405366del GRCh38
NC_000006.11:g.32373120_32373143del , CM000668.1:g.32373120_32373143del GRCh37
NC_000006.10:g.32481098_32481121del NCBI36
NG_054759.1:g.8516_8539del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374993.5:n.137+1681_137+1704del (BTNL2)
ENST00000446536.3:c.80-81_80-58del (BTNL2) ENSP00000388434.2:n.80-81_80-58del
ENST00000454136.8:c.80-78_80-55del (BTNL2) MANE Select ENSP00000390613.3:n.80-78_80-55del
ENST00000465865.6:c.80-78_80-55del (BTNL2) ENSP00000420063.1:n.80-78_80-55del
ENST00000544175.3:c.80-78_80-55del (BTNL2) ENSP00000443364.2:n.80-78_80-55del
ENST00000374993.4:c.80-78_80-55del (BTNL2) ENSP00000364132.1:n.80-78_80-55del
ENST00000446536.2:c.80-81_80-58del (BTNL2) ENSP00000388434.2:n.80-81_80-58del
ENST00000454136.7:c.80-78_80-55del (BTNL2) ENSP00000390613.3:n.80-78_80-55del
ENST00000465865.5:c.80-78_80-55del (BTNL2) ENSP00000420063.1:n.80-78_80-55del
ENST00000544175.2:c.-229-78_-229-55del (BTNL2) ENSP00000443364.1:n.-229-78_-229-55del
NM_001304561.1:c.80-78_80-55del (BTNL2) NP_001291490.1:n.80-78_80-55del
XM_011514755.1:c.80-78_80-55del (BTNL2) XP_011513057.1:n.80-78_80-55del
XM_011514756.1:c.80-78_80-55del (BTNL2) XP_011513058.1:n.80-78_80-55del
XM_011515039.1:c.482-111_482-88del (TSBP1-AS1) XP_011513341.1:n.482-111_482-88del
XR_926699.1:n.104-111_104-88del (TSBP1-AS1)
NR_136245.1:n.303-111_303-88del (TSBP1-AS1)
XM_017011057.1:c.80-78_80-55del (BTNL2) XP_016866546.1:n.80-78_80-55del
NM_001304561.2:c.80-78_80-55del (BTNL2) MANE Select NP_001291490.1:n.80-78_80-55del