Canonical Allele Identifier: CA2666008369

Gene: BAP1

Linked Data

• gnomAD v4: 3-52403010-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403011del , CM000665.2:g.52403011del	GRCh38
NC_000003.11:g.52437027del , CM000665.1:g.52437027del	GRCh37
NC_000003.10:g.52412067del	NCBI36
NG_031859.1:g.11983del , LRG_529:g.11983del

Transcript Alleles

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