Canonical Allele Identifier: CA353096409

Gene: BAP1

Linked Data

• ClinVar Variation Id: 1503671
• ClinVar RCV Id: RCV002025618
• dbSNP Id: rs2153226226
• MyVariant Identifiers: chr3:g.52436692T>C (hg19) ; chr3:g.52402676T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402676T>C , CM000665.2:g.52402676T>C	GRCh38
NC_000003.11:g.52436692T>C , CM000665.1:g.52436692T>C	GRCh37
NC_000003.10:g.52411732T>C	NCBI36
NG_031859.1:g.12318A>G , LRG_529:g.12318A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1984-2A>G MANE Select	ENSP00000417132.1:n.1984-2A>G
ENST00000296288.9:c.1930-2A>G	ENSP00000296288.5:n.1930-2A>G
ENST00000460680.5:c.1984-2A>G	ENSP00000417132.1:n.1984-2A>G
ENST00000466093.1:n.657-2A>G
ENST00000469613.5:c.183-2A>G
ENST00000478368.1:c.556-2A>G	ENSP00000420647.1:n.556-2A>G
NM_004656.3:c.1984-2A>G	NP_004647.1:n.1984-2A>G
XM_011534149.1:c.2053-2A>G	XP_011532451.1:n.2053-2A>G
XM_011534150.1:c.2008-2A>G	XP_011532452.1:n.2008-2A>G
XM_011534151.1:c.1999-2A>G	XP_011532453.1:n.1999-2A>G
XM_011534152.1:c.1939-2A>G	XP_011532454.1:n.1939-2A>G
XM_011534149.3:c.2053-2A>G	XP_011532451.1:n.2053-2A>G
XM_011534150.3:c.2008-2A>G	XP_011532452.1:n.2008-2A>G
XM_011534151.3:c.1999-2A>G	XP_011532453.1:n.1999-2A>G
XM_011534152.2:c.1939-2A>G	XP_011532454.1:n.1939-2A>G
XM_017007303.2:c.1930-2A>G	XP_016862792.1:n.1930-2A>G
NM_004656.4:c.1984-2A>G MANE Select	NP_004647.1:n.1984-2A>G