Canonical Allele Identifier: CA353801172

Gene: BTLA

Linked Data

• MyVariant Identifiers: chr3:g.112185016C>A (hg19) ; chr3:g.112466169C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466169C>A , CM000665.2:g.112466169C>A	GRCh38
NC_000003.11:g.112185016C>A , CM000665.1:g.112185016C>A	GRCh37
NC_000003.10:g.113667706C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.809G>T MANE Select	ENSP00000333919.5:p.Arg270Ile
ENST00000334529.9:c.809G>T	ENSP00000333919.5:p.Arg270Ile
ENST00000383680.4:c.665G>T	ENSP00000373178.4:p.Arg222Ile
ENST00000474965.1:n.313G>T
NM_001085357.1:c.665G>T	NP_001078826.1:p.Arg222Ile
NM_181780.3:c.809G>T	NP_861445.3:p.Arg270Ile
XM_011512446.1:c.827G>T	XP_011510748.1:p.Arg276Ile
XM_011512447.1:c.827G>T	XP_011510749.1:p.Arg276Ile
XM_011512447.3:c.827G>T	XP_011510749.1:p.Arg276Ile
XM_017005748.2:c.809G>T	XP_016861237.1:p.Arg270Ile
NM_181780.4:c.809G>T MANE Select	NP_861445.4:p.Arg270Ile
NM_001085357.2:c.665G>T	NP_001078826.1:p.Arg222Ile