Canonical Allele Identifier: CA1393855042

Gene: BTLA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466154A= , CM000665.2:g.112466154A=	GRCh38
NC_000003.11:g.112185001A= , CM000665.1:g.112185001A=	GRCh37
NC_000003.10:g.113667691A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.824T= MANE Select	ENSP00000333919.5:p.Val275=
ENST00000334529.9:c.824T=	ENSP00000333919.5:p.Val275=
ENST00000383680.4:c.680T=	ENSP00000373178.4:p.Val227=
ENST00000474965.1:n.328T=
NM_001085357.1:c.680T=	NP_001078826.1:p.Val227=
NM_181780.3:c.824T=	NP_861445.3:p.Val275=
XM_011512446.1:c.842T=	XP_011510748.1:p.Val281=
XM_011512447.1:c.842T=	XP_011510749.1:p.Val281=
XM_011512447.3:c.842T=	XP_011510749.1:p.Val281=
XM_017005748.2:c.824T=	XP_016861237.1:p.Val275=
NM_181780.4:c.824T= MANE Select	NP_861445.4:p.Val275=
NM_001085357.2:c.680T=	NP_001078826.1:p.Val227=