Canonical Allele Identifier: CA1393855028

Gene: BTLA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466116_112466117delinsTC , CM000665.2:g.112466116_112466117delinsTC	GRCh38
NC_000003.11:g.112184963_112184964delinsTC , CM000665.1:g.112184963_112184964delinsTC	GRCh37
NC_000003.10:g.113667653_113667654delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.861_862delinsGA MANE Select	ENSP00000333919.5:p.Val287=
ENST00000334529.9:c.861_862delinsGA	ENSP00000333919.5:p.Val287=
ENST00000383680.4:c.717_718delinsGA	ENSP00000373178.4:p.Val239=
ENST00000474965.1:n.365_366delinsGA
NM_001085357.1:c.717_718delinsGA	NP_001078826.1:p.Val239=
NM_181780.3:c.861_862delinsGA	NP_861445.3:p.Val287=
XM_011512446.1:c.879_880delinsGA	XP_011510748.1:p.Val293=
XM_011512447.1:c.879_880delinsGA	XP_011510749.1:p.Val293=
XM_011512447.3:c.879_880delinsGA	XP_011510749.1:p.Val293=
XM_017005748.2:c.861_862delinsGA	XP_016861237.1:p.Val287=
NM_181780.4:c.861_862delinsGA MANE Select	NP_861445.4:p.Val287=
NM_001085357.2:c.717_718delinsGA	NP_001078826.1:p.Val239=