Canonical Allele Identifier: CA353800969

Gene: BTLA

Linked Data

• MyVariant Identifiers: chr3:g.112184975A>T (hg19) ; chr3:g.112466128A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466128A>T , CM000665.2:g.112466128A>T	GRCh38
NC_000003.11:g.112184975A>T , CM000665.1:g.112184975A>T	GRCh37
NC_000003.10:g.113667665A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.850T>A MANE Select	ENSP00000333919.5:p.Ser284Thr
ENST00000334529.9:c.850T>A	ENSP00000333919.5:p.Ser284Thr
ENST00000383680.4:c.706T>A	ENSP00000373178.4:p.Ser236Thr
ENST00000474965.1:n.354T>A
NM_001085357.1:c.706T>A	NP_001078826.1:p.Ser236Thr
NM_181780.3:c.850T>A	NP_861445.3:p.Ser284Thr
XM_011512446.1:c.868T>A	XP_011510748.1:p.Ser290Thr
XM_011512447.1:c.868T>A	XP_011510749.1:p.Ser290Thr
XM_011512447.3:c.868T>A	XP_011510749.1:p.Ser290Thr
XM_017005748.2:c.850T>A	XP_016861237.1:p.Ser284Thr
NM_181780.4:c.850T>A MANE Select	NP_861445.4:p.Ser284Thr
NM_001085357.2:c.706T>A	NP_001078826.1:p.Ser236Thr