Canonical Allele Identifier: CA1393857176

Gene: BTLA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112471290G= , CM000665.2:g.112471290G=	GRCh38
NC_000003.11:g.112190137G= , CM000665.1:g.112190137G=	GRCh37
NC_000003.10:g.113672827G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_181780.4:c.469C= MANE Select	NP_861445.4:p.Arg157=
ENST00000334529.10:c.469C= MANE Select	ENSP00000333919.5:p.Arg157=
NM_001085357.1:c.404-1486C=	NP_001078826.1:n.404-1486C=
NM_001085357.2:c.404-1486C=	NP_001078826.1:n.404-1486C=
ENST00000334529.9:c.469C=	ENSP00000333919.5:p.Arg157=
ENST00000383680.4:c.404-1486C=	ENSP00000373178.4:n.404-1486C=
XM_011512446.1:c.487C=	XP_011510748.1:p.Arg163=
XM_011512447.1:c.487C=	XP_011510749.1:p.Arg163=
XM_011512447.3:c.487C=	XP_011510749.1:p.Arg163=
XM_017005748.2:c.469C=	XP_016861237.1:p.Arg157=