Canonical Allele Identifier: CA2514900160

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403033_52403034insCCGAG , CM000665.2:g.52403033_52403034insCCGAG	GRCh38
NC_000003.11:g.52437049_52437050insCCGAG , CM000665.1:g.52437049_52437050insCCGAG	GRCh37
NC_000003.10:g.52412089_52412090insCCGAG	NCBI36
NG_031859.1:g.11960_11961insCTCGG , LRG_529:g.11960_11961insCTCGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000460680.6:c.1890+104_1890+105insCTCGG MANE Select	ENSP00000417132.1:n.1890+104_1890+105insCTCGG
ENST00000296288.9:c.1836+104_1836+105insCTCGG	ENSP00000296288.5:n.1836+104_1836+105insCTCGG
ENST00000460680.5:c.1890+104_1890+105insCTCGG	ENSP00000417132.1:n.1890+104_1890+105insCTCGG
ENST00000466093.1:n.401_402insCTCGG
ENST00000469613.5:c.120-193_120-192insCTCGG
ENST00000478368.1:c.394-94_394-93insCTCGG	ENSP00000420647.1:n.394-94_394-93insCTCGG
NM_004656.3:c.1890+104_1890+105insCTCGG	NP_004647.1:n.1890+104_1890+105insCTCGG
XM_011534149.1:c.1891-94_1891-93insCTCGG	XP_011532451.1:n.1891-94_1891-93insCTCGG
XM_011534150.1:c.1846-94_1846-93insCTCGG	XP_011532452.1:n.1846-94_1846-93insCTCGG
XM_011534151.1:c.1837-94_1837-93insCTCGG	XP_011532453.1:n.1837-94_1837-93insCTCGG
XM_011534152.1:c.1845+149_1845+150insCTCGG	XP_011532454.1:n.1845+149_1845+150insCTCGG
XM_011534149.3:c.1891-94_1891-93insCTCGG	XP_011532451.1:n.1891-94_1891-93insCTCGG
XM_011534150.3:c.1846-94_1846-93insCTCGG	XP_011532452.1:n.1846-94_1846-93insCTCGG
XM_011534151.3:c.1837-94_1837-93insCTCGG	XP_011532453.1:n.1837-94_1837-93insCTCGG
XM_011534152.2:c.1845+149_1845+150insCTCGG	XP_011532454.1:n.1845+149_1845+150insCTCGG
XM_017007303.2:c.1836+104_1836+105insCTCGG	XP_016862792.1:n.1836+104_1836+105insCTCGG
NM_004656.4:c.1890+104_1890+105insCTCGG MANE Select	NP_004647.1:n.1890+104_1890+105insCTCGG