Canonical Allele Identifier: CA2678148485
Gene: BTNL2 HGNC NCBI
TSBP1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32405407_32405408insC , CM000668.2:g.32405407_32405408insC GRCh38
NC_000006.11:g.32373184_32373185insC , CM000668.1:g.32373184_32373185insC GRCh37
NC_000006.10:g.32481162_32481163insC NCBI36
NG_054759.1:g.8472_8473insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000374993.5:n.137+1637_137+1638insG (BTNL2)
ENST00000446536.3:c.80-125_80-124insG (BTNL2) ENSP00000388434.2:n.80-125_80-124insG
ENST00000454136.8:c.80-122_80-121insG (BTNL2) MANE Select ENSP00000390613.3:n.80-122_80-121insG
ENST00000465865.6:c.80-122_80-121insG (BTNL2) ENSP00000420063.1:n.80-122_80-121insG
ENST00000544175.3:c.80-122_80-121insG (BTNL2) ENSP00000443364.2:n.80-122_80-121insG
ENST00000374993.4:c.80-122_80-121insG (BTNL2) ENSP00000364132.1:n.80-122_80-121insG
ENST00000446536.2:c.80-125_80-124insG (BTNL2) ENSP00000388434.2:n.80-125_80-124insG
ENST00000454136.7:c.80-122_80-121insG (BTNL2) ENSP00000390613.3:n.80-122_80-121insG
ENST00000465865.5:c.80-122_80-121insG (BTNL2) ENSP00000420063.1:n.80-122_80-121insG
ENST00000544175.2:c.-229-122_-229-121insG (BTNL2) ENSP00000443364.1:n.-229-122_-229-121insG
NM_001304561.1:c.80-122_80-121insG (BTNL2) NP_001291490.1:n.80-122_80-121insG
XM_011514755.1:c.80-122_80-121insG (BTNL2) XP_011513057.1:n.80-122_80-121insG
XM_011514756.1:c.80-122_80-121insG (BTNL2) XP_011513058.1:n.80-122_80-121insG
XM_011515039.1:c.482-47_482-46insC (TSBP1-AS1) XP_011513341.1:n.482-47_482-46insC
XR_926699.1:n.104-47_104-46insC (TSBP1-AS1)
NR_136245.1:n.303-47_303-46insC (TSBP1-AS1)
XM_017011057.1:c.80-122_80-121insG (BTNL2) XP_016866546.1:n.80-122_80-121insG
NM_001304561.2:c.80-122_80-121insG (BTNL2) MANE Select NP_001291490.1:n.80-122_80-121insG