Canonical Allele Identifier: CA2666960702

Gene: BTLA

Linked Data

• gnomAD v4: 3-112466159-TCTTGCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466160_112466165del , CM000665.2:g.112466160_112466165del	GRCh38
NC_000003.11:g.112185007_112185012del , CM000665.1:g.112185007_112185012del	GRCh37
NC_000003.10:g.113667697_113667702del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.813_818del MANE Select	ENSP00000333919.5:p.Ala272_Arg273del
ENST00000334529.9:c.813_818del	ENSP00000333919.5:p.Ala272_Arg273del
ENST00000383680.4:c.669_674del	ENSP00000373178.4:p.Ala224_Arg225del
ENST00000474965.1:n.317_322del
NM_001085357.1:c.669_674del	NP_001078826.1:p.Ala224_Arg225del
NM_181780.3:c.813_818del	NP_861445.3:p.Ala272_Arg273del
XM_011512446.1:c.831_836del	XP_011510748.1:p.Ala278_Arg279del
XM_011512447.1:c.831_836del	XP_011510749.1:p.Ala278_Arg279del
XM_011512447.3:c.831_836del	XP_011510749.1:p.Ala278_Arg279del
XM_017005748.2:c.813_818del	XP_016861237.1:p.Ala272_Arg273del
NM_181780.4:c.813_818del MANE Select	NP_861445.4:p.Ala272_Arg273del
NM_001085357.2:c.669_674del	NP_001078826.1:p.Ala224_Arg225del