Canonical Allele Identifier: CA1619538985

Gene: BTNL2 TSBP1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32396080T= , CM000668.2:g.32396080T=	GRCh38
NC_000006.11:g.32363857T= , CM000668.1:g.32363857T=	GRCh37
NC_000006.10:g.32471835T=	NCBI36
NG_054759.1:g.17800A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000374993.5:n.465A= (BTNL2)
ENST00000454136.8:c.1037A= (BTNL2) MANE Select	ENSP00000390613.3:p.Asp346=
ENST00000465865.6:c.*312A= (BTNL2)	ENSP00000420063.1:n.*312A=
ENST00000544175.3:c.*298A= (BTNL2)	ENSP00000443364.2:n.*298A=
ENST00000374993.4:c.1037A= (BTNL2)	ENSP00000364132.1:p.Asp346=
ENST00000454136.7:c.1037A= (BTNL2)	ENSP00000390613.3:p.Asp346=
ENST00000465865.5:c.519A= (BTNL2)	ENSP00000420063.1:n.519A=
ENST00000544175.2:c.206A= (BTNL2)	ENSP00000443364.1:p.Asp69=
NM_001304561.1:c.1037A= (BTNL2)	NP_001291490.1:p.Asp346=
XM_011514755.1:c.1037A= (BTNL2)	XP_011513057.1:p.Asp346=
XM_011514756.1:c.755A= (BTNL2)	XP_011513058.1:p.Asp252=
XM_011515039.1:c.482-9374T= (TSBP1-AS1)	XP_011513341.1:n.482-9374T=
NR_136245.1:n.303-9374T= (TSBP1-AS1)
XM_017011057.1:c.1037A= (BTNL2)	XP_016866546.1:p.Asp346=
NM_001304561.2:c.1037A= (BTNL2) MANE Select	NP_001291490.1:p.Asp346=