Canonical Allele Identifier: CA2581566576

Gene: BTNL2 TSBP1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32400239G>T , CM000668.2:g.32400239G>T	GRCh38
NC_000006.11:g.32368016G>T , CM000668.1:g.32368016G>T	GRCh37
NC_000006.10:g.32475994G>T	NCBI36
NG_054759.1:g.13641C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374993.5:n.158+1546C>A (BTNL2)
ENST00000454136.8:c.730+1546C>A (BTNL2) MANE Select	ENSP00000390613.3:n.730+1546C>A
ENST00000465865.6:c.*5+1546C>A (BTNL2)	ENSP00000420063.1:n.*5+1546C>A
ENST00000544175.3:c.207+1546C>A (BTNL2)	ENSP00000443364.2:n.207+1546C>A
ENST00000374993.4:c.730+1546C>A (BTNL2)	ENSP00000364132.1:n.730+1546C>A
ENST00000454136.7:c.730+1546C>A (BTNL2)	ENSP00000390613.3:n.730+1546C>A
ENST00000465865.5:c.212+1546C>A (BTNL2)	ENSP00000420063.1:n.212+1546C>A
ENST00000544175.2:c.-102+1546C>A (BTNL2)	ENSP00000443364.1:n.-102+1546C>A
NM_001304561.1:c.730+1546C>A (BTNL2)	NP_001291490.1:n.730+1546C>A
XM_011514755.1:c.730+1546C>A (BTNL2)	XP_011513057.1:n.730+1546C>A
XM_011514756.1:c.448+1546C>A (BTNL2)	XP_011513058.1:n.448+1546C>A
XM_011515039.1:c.482-5215G>T (TSBP1-AS1)	XP_011513341.1:n.482-5215G>T
NR_136245.1:n.303-5215G>T (TSBP1-AS1)
XM_017011057.1:c.730+1546C>A (BTNL2)	XP_016866546.1:n.730+1546C>A
NM_001304561.2:c.730+1546C>A (BTNL2) MANE Select	NP_001291490.1:n.730+1546C>A