Canonical Allele Identifier: CA353800890

Gene: BTLA

Linked Data

• MyVariant Identifiers: chr3:g.112184955T>G (hg19) ; chr3:g.112466108T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466108T>G , CM000665.2:g.112466108T>G	GRCh38
NC_000003.11:g.112184955T>G , CM000665.1:g.112184955T>G	GRCh37
NC_000003.10:g.113667645T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.870A>C MANE Select	ENSP00000333919.5:p.Ter290Tyr
ENST00000334529.9:c.870A>C	ENSP00000333919.5:p.Ter290Tyr
ENST00000383680.4:c.726A>C	ENSP00000373178.4:p.Ter242Tyr
ENST00000474965.1:n.374A>C
NM_001085357.1:c.726A>C	NP_001078826.1:p.Ter242Tyr
NM_181780.3:c.870A>C	NP_861445.3:p.Ter290Tyr
XM_011512446.1:c.888A>C	XP_011510748.1:p.Ter296Tyr
XM_011512447.1:c.888A>C	XP_011510749.1:p.Ter296Tyr
XM_011512447.3:c.888A>C	XP_011510749.1:p.Ter296Tyr
XM_017005748.2:c.870A>C	XP_016861237.1:p.Ter290Tyr
NM_181780.4:c.870A>C MANE Select	NP_861445.4:p.Ter290Tyr
NM_001085357.2:c.726A>C	NP_001078826.1:p.Ter242Tyr