Canonical Allele Identifier: CA363565020
Gene: BTNL2 HGNC NCBI
TSBP1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32396087C>A , CM000668.2:g.32396087C>A GRCh38
NC_000006.11:g.32363864C>A , CM000668.1:g.32363864C>A GRCh37
NC_000006.10:g.32471842C>A NCBI36
NG_054759.1:g.17793G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374993.5:n.458G>T (BTNL2)
ENST00000454136.8:c.1030G>T (BTNL2) MANE Select ENSP00000390613.3:p.Glu344Ter
ENST00000465865.6:c.*305G>T (BTNL2) ENSP00000420063.1:n.*305G>T
ENST00000544175.3:c.*291G>T (BTNL2) ENSP00000443364.2:n.*291G>T
ENST00000374993.4:c.1030G>T (BTNL2) ENSP00000364132.1:p.Glu344Ter
ENST00000454136.7:c.1030G>T (BTNL2) ENSP00000390613.3:p.Glu344Ter
ENST00000465865.5:c.512G>T (BTNL2) ENSP00000420063.1:n.512G>T
ENST00000544175.2:c.199G>T (BTNL2) ENSP00000443364.1:p.Glu67Ter
NM_001304561.1:c.1030G>T (BTNL2) NP_001291490.1:p.Glu344Ter
XM_011514755.1:c.1030G>T (BTNL2) XP_011513057.1:p.Glu344Ter
XM_011514756.1:c.748G>T (BTNL2) XP_011513058.1:p.Glu250Ter
XM_011515039.1:c.482-9367C>A (TSBP1-AS1) XP_011513341.1:n.482-9367C>A
NR_136245.1:n.303-9367C>A (TSBP1-AS1)
XM_017011057.1:c.1030G>T (BTNL2) XP_016866546.1:p.Glu344Ter
NM_001304561.2:c.1030G>T (BTNL2) MANE Select NP_001291490.1:p.Glu344Ter