Canonical Allele Identifier: CA1393855048
Gene: BTLA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.112466176T= , CM000665.2:g.112466176T= GRCh38
NC_000003.11:g.112185023T= , CM000665.1:g.112185023T= GRCh37
NC_000003.10:g.113667713T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000334529.10:c.802A= MANE Select ENSP00000333919.5:p.Asn268=
ENST00000334529.9:c.802A= ENSP00000333919.5:p.Asn268=
ENST00000383680.4:c.658A= ENSP00000373178.4:p.Asn220=
ENST00000474965.1:n.306A=
NM_001085357.1:c.658A= NP_001078826.1:p.Asn220=
NM_181780.3:c.802A= NP_861445.3:p.Asn268=
XM_011512446.1:c.820A= XP_011510748.1:p.Asn274=
XM_011512447.1:c.820A= XP_011510749.1:p.Asn274=
XM_011512447.3:c.820A= XP_011510749.1:p.Asn274=
XM_017005748.2:c.802A= XP_016861237.1:p.Asn268=
NM_181780.4:c.802A= MANE Select NP_861445.4:p.Asn268=
NM_001085357.2:c.658A= NP_001078826.1:p.Asn220=