Canonical Allele Identifier: CA1393855029

Gene: BTLA

Linked Data

• dbSNP Id: rs2082224748

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.861del MANE Select	ENSP00000333919.5:p.Arg288GlyfsTer13
ENST00000334529.9:c.861del	ENSP00000333919.5:p.Arg288GlyfsTer13
ENST00000383680.4:c.717del	ENSP00000373178.4:p.Arg240GlyfsTer?
ENST00000474965.1:n.365del
NM_001085357.1:c.717del	NP_001078826.1:p.Arg240GlyfsTer13
NM_181780.3:c.861del	NP_861445.3:p.Arg288GlyfsTer13
XM_011512446.1:c.879del	XP_011510748.1:p.Arg294GlyfsTer13
XM_011512447.1:c.879del	XP_011510749.1:p.Arg294GlyfsTer13
XM_011512447.3:c.879del	XP_011510749.1:p.Arg294GlyfsTer13
XM_017005748.2:c.861del	XP_016861237.1:p.Arg288GlyfsTer13
NM_181780.4:c.861del MANE Select	NP_861445.4:p.Arg288GlyfsTer13
NM_001085357.2:c.717del	NP_001078826.1:p.Arg240GlyfsTer13