Canonical Allele Identifier: CA1619538983

Gene: BTNL2 TSBP1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32396069G= , CM000668.2:g.32396069G=	GRCh38
NC_000006.11:g.32363846G= , CM000668.1:g.32363846G=	GRCh37
NC_000006.10:g.32471824G=	NCBI36
NG_054759.1:g.17811C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374993.5:n.476C= (BTNL2)
ENST00000454136.8:c.1048C= (BTNL2) MANE Select	ENSP00000390613.3:p.Gln350=
ENST00000465865.6:c.*323C= (BTNL2)	ENSP00000420063.1:n.*323C=
ENST00000544175.3:c.*309C= (BTNL2)	ENSP00000443364.2:n.*309C=
ENST00000374993.4:c.1048C= (BTNL2)	ENSP00000364132.1:p.Gln350=
ENST00000454136.7:c.1048C= (BTNL2)	ENSP00000390613.3:p.Gln350=
ENST00000465865.5:c.530C= (BTNL2)	ENSP00000420063.1:n.530C=
ENST00000544175.2:c.217C= (BTNL2)	ENSP00000443364.1:p.Gln73=
NM_001304561.1:c.1048C= (BTNL2)	NP_001291490.1:p.Gln350=
XM_011514755.1:c.1048C= (BTNL2)	XP_011513057.1:p.Gln350=
XM_011514756.1:c.766C= (BTNL2)	XP_011513058.1:p.Gln256=
XM_011515039.1:c.482-9385G= (TSBP1-AS1)	XP_011513341.1:n.482-9385G=
NR_136245.1:n.303-9385G= (TSBP1-AS1)
XM_017011057.1:c.1048C= (BTNL2)	XP_016866546.1:p.Gln350=
NM_001304561.2:c.1048C= (BTNL2) MANE Select	NP_001291490.1:p.Gln350=