Canonical Allele Identifier: CA1393855030

Gene: BTLA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466117C= , CM000665.2:g.112466117C=	GRCh38
NC_000003.11:g.112184964C= , CM000665.1:g.112184964C=	GRCh37
NC_000003.10:g.113667654C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.861G= MANE Select	ENSP00000333919.5:p.Val287=
ENST00000334529.9:c.861G=	ENSP00000333919.5:p.Val287=
ENST00000383680.4:c.717G=	ENSP00000373178.4:p.Val239=
ENST00000474965.1:n.365G=
NM_001085357.1:c.717G=	NP_001078826.1:p.Val239=
NM_181780.3:c.861G=	NP_861445.3:p.Val287=
XM_011512446.1:c.879G=	XP_011510748.1:p.Val293=
XM_011512447.1:c.879G=	XP_011510749.1:p.Val293=
XM_011512447.3:c.879G=	XP_011510749.1:p.Val293=
XM_017005748.2:c.861G=	XP_016861237.1:p.Val287=
NM_181780.4:c.861G= MANE Select	NP_861445.4:p.Val287=
NM_001085357.2:c.717G=	NP_001078826.1:p.Val239=