Canonical Allele Identifier: CA2666008400

Gene: BAP1

Linked Data

• gnomAD v4: 3-52403027-G-GCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403031_52403033dup , CM000665.2:g.52403031_52403033dup	GRCh38
NC_000003.11:g.52437047_52437049dup , CM000665.1:g.52437047_52437049dup	GRCh37
NC_000003.10:g.52412087_52412089dup	NCBI36
NG_031859.1:g.11964_11966dup , LRG_529:g.11964_11966dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000460680.6:c.1890+108_1890+110dup MANE Select	ENSP00000417132.1:n.1890+108_1890+110dup
ENST00000296288.9:c.1836+108_1836+110dup	ENSP00000296288.5:n.1836+108_1836+110dup
ENST00000460680.5:c.1890+108_1890+110dup	ENSP00000417132.1:n.1890+108_1890+110dup
ENST00000466093.1:n.405_407dup
ENST00000469613.5:c.120-189_120-187dup
ENST00000478368.1:c.394-90_394-88dup	ENSP00000420647.1:n.394-90_394-88dup
NM_004656.3:c.1890+108_1890+110dup	NP_004647.1:n.1890+108_1890+110dup
XM_011534149.1:c.1891-90_1891-88dup	XP_011532451.1:n.1891-90_1891-88dup
XM_011534150.1:c.1846-90_1846-88dup	XP_011532452.1:n.1846-90_1846-88dup
XM_011534151.1:c.1837-90_1837-88dup	XP_011532453.1:n.1837-90_1837-88dup
XM_011534152.1:c.1845+153_1845+155dup	XP_011532454.1:n.1845+153_1845+155dup
XM_011534149.3:c.1891-90_1891-88dup	XP_011532451.1:n.1891-90_1891-88dup
XM_011534150.3:c.1846-90_1846-88dup	XP_011532452.1:n.1846-90_1846-88dup
XM_011534151.3:c.1837-90_1837-88dup	XP_011532453.1:n.1837-90_1837-88dup
XM_011534152.2:c.1845+153_1845+155dup	XP_011532454.1:n.1845+153_1845+155dup
XM_017007303.2:c.1836+108_1836+110dup	XP_016862792.1:n.1836+108_1836+110dup
NM_004656.4:c.1890+108_1890+110dup MANE Select	NP_004647.1:n.1890+108_1890+110dup