Canonical Allele Identifier: CA2436636
Gene: BAP1 HGNC NCBI

Linked Data

dbSNP Id: rs757077441
gnomAD v2: 3-52436732-G-A
gnomAD v4: 3-52402716-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52402716G>A , CM000665.2:g.52402716G>A GRCh38
NC_000003.11:g.52436732G>A , CM000665.1:g.52436732G>A GRCh37
NC_000003.10:g.52411772G>A NCBI36
NG_031859.1:g.12278C>T , LRG_529:g.12278C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000460680.6:c.1984-42C>T MANE Select ENSP00000417132.1:n.1984-42C>T
ENST00000296288.9:c.1930-42C>T ENSP00000296288.5:n.1930-42C>T
ENST00000460680.5:c.1984-42C>T ENSP00000417132.1:n.1984-42C>T
ENST00000466093.1:n.657-42C>T
ENST00000469613.5:c.183-42C>T
ENST00000478368.1:c.556-42C>T ENSP00000420647.1:n.556-42C>T
NM_004656.3:c.1984-42C>T NP_004647.1:n.1984-42C>T
XM_011534149.1:c.2053-42C>T XP_011532451.1:n.2053-42C>T
XM_011534150.1:c.2008-42C>T XP_011532452.1:n.2008-42C>T
XM_011534151.1:c.1999-42C>T XP_011532453.1:n.1999-42C>T
XM_011534152.1:c.1939-42C>T XP_011532454.1:n.1939-42C>T
XM_011534149.3:c.2053-42C>T XP_011532451.1:n.2053-42C>T
XM_011534150.3:c.2008-42C>T XP_011532452.1:n.2008-42C>T
XM_011534151.3:c.1999-42C>T XP_011532453.1:n.1999-42C>T
XM_011534152.2:c.1939-42C>T XP_011532454.1:n.1939-42C>T
XM_017007303.2:c.1930-42C>T XP_016862792.1:n.1930-42C>T
NM_004656.4:c.1984-42C>T MANE Select NP_004647.1:n.1984-42C>T