Canonical Allele Identifier: CA2756265857

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403052dup , CM000665.2:g.52403052dup	GRCh38
NC_000003.11:g.52437068dup , CM000665.1:g.52437068dup	GRCh37
NC_000003.10:g.52412108dup	NCBI36
NG_031859.1:g.11943dup , LRG_529:g.11943dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1890+87dup MANE Select	ENSP00000417132.1:n.1890+87dup
ENST00000296288.9:c.1836+87dup	ENSP00000296288.5:n.1836+87dup
ENST00000460680.5:c.1890+87dup	ENSP00000417132.1:n.1890+87dup
ENST00000466093.1:n.384dup
ENST00000469613.5:c.120-210dup
ENST00000478368.1:c.393+87dup	ENSP00000420647.1:n.393+87dup
NM_004656.3:c.1890+87dup	NP_004647.1:n.1890+87dup
XM_011534149.1:c.1890+87dup	XP_011532451.1:n.1890+87dup
XM_011534150.1:c.1846-111dup	XP_011532452.1:n.1846-111dup
XM_011534151.1:c.1836+87dup	XP_011532453.1:n.1836+87dup
XM_011534152.1:c.1845+132dup	XP_011532454.1:n.1845+132dup
XM_011534149.3:c.1890+87dup	XP_011532451.1:n.1890+87dup
XM_011534150.3:c.1846-111dup	XP_011532452.1:n.1846-111dup
XM_011534151.3:c.1836+87dup	XP_011532453.1:n.1836+87dup
XM_011534152.2:c.1845+132dup	XP_011532454.1:n.1845+132dup
XM_017007303.2:c.1836+87dup	XP_016862792.1:n.1836+87dup
NM_004656.4:c.1890+87dup MANE Select	NP_004647.1:n.1890+87dup