Canonical Allele Identifier: CA1393855022
Gene: BTLA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.112466105_112466110delinsGACTTA , CM000665.2:g.112466105_112466110delinsGACTTA GRCh38
NC_000003.11:g.112184952_112184957delinsGACTTA , CM000665.1:g.112184952_112184957delinsGACTTA GRCh37
NC_000003.10:g.113667642_113667647delinsGACTTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000334529.10:c.868_*3delinsTAAGTC MANE Select ENSP00000333919.5:n.[c.868_*3delinsTAAGTC;Ter290=]
ENST00000334529.9:c.868_*3delinsTAAGTC ENSP00000333919.5:n.[c.868_*3delinsTAAGTC;Ter290=]
ENST00000474965.1:n.372_377delinsTAAGTC
NM_001085357.1:c.724_*3delinsTAAGTC NP_001078826.1:n.[c.724_*3delinsTAAGTC;Ter242=]
NM_181780.3:c.868_*3delinsTAAGTC NP_861445.3:n.[c.868_*3delinsTAAGTC;Ter290=]
XM_011512446.1:c.886_*3delinsTAAGTC XP_011510748.1:n.[c.886_*3delinsTAAGTC;Ter296=]
XM_011512447.1:c.886_*3delinsTAAGTC XP_011510749.1:n.[c.886_*3delinsTAAGTC;Ter296=]
XM_011512447.3:c.886_*3delinsTAAGTC XP_011510749.1:n.[c.886_*3delinsTAAGTC;Ter296=]
XM_017005748.2:c.868_*3delinsTAAGTC XP_016861237.1:n.[c.868_*3delinsTAAGTC;Ter290=]
NM_181780.4:c.868_*3delinsTAAGTC MANE Select NP_861445.4:n.[c.868_*3delinsTAAGTC;Ter290=]
NM_001085357.2:c.724_*3delinsTAAGTC NP_001078826.1:n.[c.724_*3delinsTAAGTC;Ter242=]