Canonical Allele Identifier: CA353096368

Gene: BAP1

Linked Data

• dbSNP Id: rs1553644633
• MyVariant Identifiers: chr3:g.52436682G>T (hg19) ; chr3:g.52402666G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402666G>T , CM000665.2:g.52402666G>T	GRCh38
NC_000003.11:g.52436682G>T , CM000665.1:g.52436682G>T	GRCh37
NC_000003.10:g.52411722G>T	NCBI36
NG_031859.1:g.12328C>A , LRG_529:g.12328C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1992C>A MANE Select	ENSP00000417132.1:p.Asp664Glu
ENST00000296288.9:c.1938C>A	ENSP00000296288.5:p.Asp646Glu
ENST00000460680.5:c.1992C>A	ENSP00000417132.1:p.Asp664Glu
ENST00000466093.1:n.665C>A
ENST00000469613.5:c.191C>A
ENST00000478368.1:c.564C>A	ENSP00000420647.1:p.Asp188Glu
NM_004656.3:c.1992C>A	NP_004647.1:p.Asp664Glu
XM_011534149.1:c.2061C>A	XP_011532451.1:p.Asp687Glu
XM_011534150.1:c.2016C>A	XP_011532452.1:p.Asp672Glu
XM_011534151.1:c.2007C>A	XP_011532453.1:p.Asp669Glu
XM_011534152.1:c.1947C>A	XP_011532454.1:p.Asp649Glu
XM_011534149.3:c.2061C>A	XP_011532451.1:p.Asp687Glu
XM_011534150.3:c.2016C>A	XP_011532452.1:p.Asp672Glu
XM_011534151.3:c.2007C>A	XP_011532453.1:p.Asp669Glu
XM_011534152.2:c.1947C>A	XP_011532454.1:p.Asp649Glu
XM_017007303.2:c.1938C>A	XP_016862792.1:p.Asp646Glu
NM_004656.4:c.1992C>A MANE Select	NP_004647.1:p.Asp664Glu