Canonical Allele Identifier: CA353801037

Gene: BTLA

Linked Data

• gnomAD v4: 3-112466143-G-T
• MyVariant Identifiers: chr3:g.112184990G>T (hg19) ; chr3:g.112466143G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466143G>T , CM000665.2:g.112466143G>T	GRCh38
NC_000003.11:g.112184990G>T , CM000665.1:g.112184990G>T	GRCh37
NC_000003.10:g.113667680G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.835C>A MANE Select	ENSP00000333919.5:p.Pro279Thr
ENST00000334529.9:c.835C>A	ENSP00000333919.5:p.Pro279Thr
ENST00000383680.4:c.691C>A	ENSP00000373178.4:p.Pro231Thr
ENST00000474965.1:n.339C>A
NM_001085357.1:c.691C>A	NP_001078826.1:p.Pro231Thr
NM_181780.3:c.835C>A	NP_861445.3:p.Pro279Thr
XM_011512446.1:c.853C>A	XP_011510748.1:p.Pro285Thr
XM_011512447.1:c.853C>A	XP_011510749.1:p.Pro285Thr
XM_011512447.3:c.853C>A	XP_011510749.1:p.Pro285Thr
XM_017005748.2:c.835C>A	XP_016861237.1:p.Pro279Thr
NM_181780.4:c.835C>A MANE Select	NP_861445.4:p.Pro279Thr
NM_001085357.2:c.691C>A	NP_001078826.1:p.Pro231Thr