Canonical Allele Identifier: CA80779551

Gene: BTLA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112498887G>A , CM000665.2:g.112498887G>A	GRCh38
NC_000003.11:g.112217734G>A , CM000665.1:g.112217734G>A	GRCh37
NC_000003.10:g.113700424G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.88+384C>T MANE Select	ENSP00000333919.5:n.88+384C>T
ENST00000334529.9:c.88+384C>T	ENSP00000333919.5:n.88+384C>T
ENST00000383680.4:c.88+384C>T	ENSP00000373178.4:n.88+384C>T
NM_001085357.1:c.88+384C>T	NP_001078826.1:n.88+384C>T
NM_181780.3:c.88+384C>T	NP_861445.3:n.88+384C>T
XM_011512446.1:c.88+384C>T	XP_011510748.1:n.88+384C>T
XM_011512447.1:c.88+384C>T	XP_011510749.1:n.88+384C>T
XM_011512447.3:c.88+384C>T	XP_011510749.1:n.88+384C>T
XM_017005748.2:c.88+384C>T	XP_016861237.1:n.88+384C>T
NM_181780.4:c.88+384C>T MANE Select	NP_861445.4:n.88+384C>T
NM_001085357.2:c.88+384C>T	NP_001078826.1:n.88+384C>T