Canonical Allele Identifier: CA2559739609

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403011C>T , CM000665.2:g.52403011C>T	GRCh38
NC_000003.11:g.52437027C>T , CM000665.1:g.52437027C>T	GRCh37
NC_000003.10:g.52412067C>T	NCBI36
NG_031859.1:g.11983G>A , LRG_529:g.11983G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1890+127G>A MANE Select	ENSP00000417132.1:n.1890+127G>A
ENST00000296288.9:c.1836+127G>A	ENSP00000296288.5:n.1836+127G>A
ENST00000460680.5:c.1890+127G>A	ENSP00000417132.1:n.1890+127G>A
ENST00000466093.1:n.424G>A
ENST00000469613.5:c.120-170G>A
ENST00000478368.1:c.394-71G>A	ENSP00000420647.1:n.394-71G>A
NM_004656.3:c.1890+127G>A	NP_004647.1:n.1890+127G>A
XM_011534149.1:c.1891-71G>A	XP_011532451.1:n.1891-71G>A
XM_011534150.1:c.1846-71G>A	XP_011532452.1:n.1846-71G>A
XM_011534151.1:c.1837-71G>A	XP_011532453.1:n.1837-71G>A
XM_011534152.1:c.1846-140G>A	XP_011532454.1:n.1846-140G>A
XM_011534149.3:c.1891-71G>A	XP_011532451.1:n.1891-71G>A
XM_011534150.3:c.1846-71G>A	XP_011532452.1:n.1846-71G>A
XM_011534151.3:c.1837-71G>A	XP_011532453.1:n.1837-71G>A
XM_011534152.2:c.1846-140G>A	XP_011532454.1:n.1846-140G>A
XM_017007303.2:c.1836+127G>A	XP_016862792.1:n.1836+127G>A
NM_004656.4:c.1890+127G>A MANE Select	NP_004647.1:n.1890+127G>A