Canonical Allele Identifier: CA1393855014

Gene: BTLA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466087C= , CM000665.2:g.112466087C=	GRCh38
NC_000003.11:g.112184934C= , CM000665.1:g.112184934C=	GRCh37
NC_000003.10:g.113667624C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.*21G= MANE Select	ENSP00000333919.5:n.*21G=
ENST00000334529.9:c.*21G=	ENSP00000333919.5:n.*21G=
ENST00000474965.1:n.395G=
NM_001085357.1:c.*21G=	NP_001078826.1:n.*21G=
NM_181780.3:c.*21G=	NP_861445.3:n.*21G=
XM_011512446.1:c.*21G=	XP_011510748.1:n.*21G=
XM_011512447.1:c.*21G=	XP_011510749.1:n.*21G=
XM_011512447.3:c.*21G=	XP_011510749.1:n.*21G=
XM_017005748.2:c.*21G=	XP_016861237.1:n.*21G=
NM_181780.4:c.*21G= MANE Select	NP_861445.4:n.*21G=
NM_001085357.2:c.*21G=	NP_001078826.1:n.*21G=