Canonical Allele Identifier: CA2756265844

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402995_52402996insCCCC , CM000665.2:g.52402995_52402996insCCCC	GRCh38
NC_000003.11:g.52437011_52437012insCCCC , CM000665.1:g.52437011_52437012insCCCC	GRCh37
NC_000003.10:g.52412051_52412052insCCCC	NCBI36
NG_031859.1:g.12001_12002insGGGG , LRG_529:g.12001_12002insGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1891-122_1891-121insGGGG MANE Select	ENSP00000417132.1:n.1891-122_1891-121insGGGG
ENST00000296288.9:c.1837-122_1837-121insGGGG	ENSP00000296288.5:n.1837-122_1837-121insGGGG
ENST00000460680.5:c.1891-122_1891-121insGGGG	ENSP00000417132.1:n.1891-122_1891-121insGGGG
ENST00000466093.1:n.442_443insGGGG
ENST00000469613.5:c.120-152_120-151insGGGG
ENST00000478368.1:c.394-53_394-52insGGGG	ENSP00000420647.1:n.394-53_394-52insGGGG
NM_004656.3:c.1891-122_1891-121insGGGG	NP_004647.1:n.1891-122_1891-121insGGGG
XM_011534149.1:c.1891-53_1891-52insGGGG	XP_011532451.1:n.1891-53_1891-52insGGGG
XM_011534150.1:c.1846-53_1846-52insGGGG	XP_011532452.1:n.1846-53_1846-52insGGGG
XM_011534151.1:c.1837-53_1837-52insGGGG	XP_011532453.1:n.1837-53_1837-52insGGGG
XM_011534152.1:c.1846-122_1846-121insGGGG	XP_011532454.1:n.1846-122_1846-121insGGGG
XM_011534149.3:c.1891-53_1891-52insGGGG	XP_011532451.1:n.1891-53_1891-52insGGGG
XM_011534150.3:c.1846-53_1846-52insGGGG	XP_011532452.1:n.1846-53_1846-52insGGGG
XM_011534151.3:c.1837-53_1837-52insGGGG	XP_011532453.1:n.1837-53_1837-52insGGGG
XM_011534152.2:c.1846-122_1846-121insGGGG	XP_011532454.1:n.1846-122_1846-121insGGGG
XM_017007303.2:c.1837-122_1837-121insGGGG	XP_016862792.1:n.1837-122_1837-121insGGGG
NM_004656.4:c.1891-122_1891-121insGGGG MANE Select	NP_004647.1:n.1891-122_1891-121insGGGG