Canonical Allele Identifier: CA1393859717

Gene: BTLA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112477584T= , CM000665.2:g.112477584T=	GRCh38
NC_000003.11:g.112196431T= , CM000665.1:g.112196431T=	GRCh37
NC_000003.10:g.113679121T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_181780.4:c.403+1871A= MANE Select	NP_861445.4:n.403+1871A=
ENST00000334529.10:c.403+1871A= MANE Select	ENSP00000333919.5:n.403+1871A=
NM_001085357.1:c.403+1871A=	NP_001078826.1:n.403+1871A=
NM_001085357.2:c.403+1871A=	NP_001078826.1:n.403+1871A=
NM_181780.3:c.403+1871A=	NP_861445.3:n.403+1871A=
ENST00000334529.9:c.403+1871A=	ENSP00000333919.5:n.403+1871A=
ENST00000383680.4:c.403+1871A=	ENSP00000373178.4:n.403+1871A=
XM_011512446.1:c.403+1871A=	XP_011510748.1:n.403+1871A=
XM_011512447.1:c.403+1871A=	XP_011510749.1:n.403+1871A=
XM_011512447.3:c.403+1871A=	XP_011510749.1:n.403+1871A=
XM_017005748.2:c.403+1871A=	XP_016861237.1:n.403+1871A=