Canonical Allele Identifier: CA353800987

Gene: BTLA

Linked Data

• MyVariant Identifiers: chr3:g.112184979A>C (hg19) ; chr3:g.112466132A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466132A>C , CM000665.2:g.112466132A>C	GRCh38
NC_000003.11:g.112184979A>C , CM000665.1:g.112184979A>C	GRCh37
NC_000003.10:g.113667669A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.846T>G MANE Select	ENSP00000333919.5:p.Tyr282Ter
ENST00000334529.9:c.846T>G	ENSP00000333919.5:p.Tyr282Ter
ENST00000383680.4:c.702T>G	ENSP00000373178.4:p.Tyr234Ter
ENST00000474965.1:n.350T>G
NM_001085357.1:c.702T>G	NP_001078826.1:p.Tyr234Ter
NM_181780.3:c.846T>G	NP_861445.3:p.Tyr282Ter
XM_011512446.1:c.864T>G	XP_011510748.1:p.Tyr288Ter
XM_011512447.1:c.864T>G	XP_011510749.1:p.Tyr288Ter
XM_011512447.3:c.864T>G	XP_011510749.1:p.Tyr288Ter
XM_017005748.2:c.846T>G	XP_016861237.1:p.Tyr282Ter
NM_181780.4:c.846T>G MANE Select	NP_861445.4:p.Tyr282Ter
NM_001085357.2:c.702T>G	NP_001078826.1:p.Tyr234Ter