Canonical Allele Identifier: CA353800928

Gene: BTLA

Linked Data

• gnomAD v4: 3-112466119-C-A
• MyVariant Identifiers: chr3:g.112184966C>A (hg19) ; chr3:g.112466119C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466119C>A , CM000665.2:g.112466119C>A	GRCh38
NC_000003.11:g.112184966C>A , CM000665.1:g.112184966C>A	GRCh37
NC_000003.10:g.113667656C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.859G>T MANE Select	ENSP00000333919.5:p.Val287Leu
ENST00000334529.9:c.859G>T	ENSP00000333919.5:p.Val287Leu
ENST00000383680.4:c.715G>T	ENSP00000373178.4:p.Val239Leu
ENST00000474965.1:n.363G>T
NM_001085357.1:c.715G>T	NP_001078826.1:p.Val239Leu
NM_181780.3:c.859G>T	NP_861445.3:p.Val287Leu
XM_011512446.1:c.877G>T	XP_011510748.1:p.Val293Leu
XM_011512447.1:c.877G>T	XP_011510749.1:p.Val293Leu
XM_011512447.3:c.877G>T	XP_011510749.1:p.Val293Leu
XM_017005748.2:c.859G>T	XP_016861237.1:p.Val287Leu
NM_181780.4:c.859G>T MANE Select	NP_861445.4:p.Val287Leu
NM_001085357.2:c.715G>T	NP_001078826.1:p.Val239Leu