Canonical Allele Identifier: CA353800953

Gene: BTLA

Linked Data

• MyVariant Identifiers: chr3:g.112184971A>C (hg19) ; chr3:g.112466124A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466124A>C , CM000665.2:g.112466124A>C	GRCh38
NC_000003.11:g.112184971A>C , CM000665.1:g.112184971A>C	GRCh37
NC_000003.10:g.113667661A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.854T>G MANE Select	ENSP00000333919.5:p.Ile285Arg
ENST00000334529.9:c.854T>G	ENSP00000333919.5:p.Ile285Arg
ENST00000383680.4:c.710T>G	ENSP00000373178.4:p.Ile237Arg
ENST00000474965.1:n.358T>G
NM_001085357.1:c.710T>G	NP_001078826.1:p.Ile237Arg
NM_181780.3:c.854T>G	NP_861445.3:p.Ile285Arg
XM_011512446.1:c.872T>G	XP_011510748.1:p.Ile291Arg
XM_011512447.1:c.872T>G	XP_011510749.1:p.Ile291Arg
XM_011512447.3:c.872T>G	XP_011510749.1:p.Ile291Arg
XM_017005748.2:c.854T>G	XP_016861237.1:p.Ile285Arg
NM_181780.4:c.854T>G MANE Select	NP_861445.4:p.Ile285Arg
NM_001085357.2:c.710T>G	NP_001078826.1:p.Ile237Arg