Canonical Allele Identifier: CA353801041

Gene: BTLA

Linked Data

• gnomAD v4: 3-112466145-G-C
• MyVariant Identifiers: chr3:g.112184992G>C (hg19) ; chr3:g.112466145G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466145G>C , CM000665.2:g.112466145G>C	GRCh38
NC_000003.11:g.112184992G>C , CM000665.1:g.112184992G>C	GRCh37
NC_000003.10:g.113667682G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.833C>G MANE Select	ENSP00000333919.5:p.Ala278Gly
ENST00000334529.9:c.833C>G	ENSP00000333919.5:p.Ala278Gly
ENST00000383680.4:c.689C>G	ENSP00000373178.4:p.Ala230Gly
ENST00000474965.1:n.337C>G
NM_001085357.1:c.689C>G	NP_001078826.1:p.Ala230Gly
NM_181780.3:c.833C>G	NP_861445.3:p.Ala278Gly
XM_011512446.1:c.851C>G	XP_011510748.1:p.Ala284Gly
XM_011512447.1:c.851C>G	XP_011510749.1:p.Ala284Gly
XM_011512447.3:c.851C>G	XP_011510749.1:p.Ala284Gly
XM_017005748.2:c.833C>G	XP_016861237.1:p.Ala278Gly
NM_181780.4:c.833C>G MANE Select	NP_861445.4:p.Ala278Gly
NM_001085357.2:c.689C>G	NP_001078826.1:p.Ala230Gly