Canonical Allele Identifier: CA129101
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 30300
dbSNP Id: rs587776878

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52402423T>C , CM000665.2:g.52402423T>C GRCh38
NC_000003.11:g.52436439T>C , CM000665.1:g.52436439T>C GRCh37
NC_000003.10:g.52411479T>C NCBI36
NG_031859.1:g.12571A>G , LRG_529:g.12571A>G
NG_052911.1:g.91105T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000460680.6:c.2057-2A>G MANE Select ENSP00000417132.1:n.2057-2A>G
ENST00000296288.9:c.2003-2A>G ENSP00000296288.5:n.2003-2A>G
ENST00000460680.5:c.2057-2A>G ENSP00000417132.1:n.2057-2A>G
ENST00000466093.1:n.730-2A>G
ENST00000469613.5:c.256-2A>G
ENST00000478368.1:c.629-2A>G ENSP00000420647.1:n.629-2A>G
NM_004656.3:c.2057-2A>G NP_004647.1:n.2057-2A>G
XM_011534149.1:c.2126-2A>G XP_011532451.1:n.2126-2A>G
XM_011534150.1:c.2081-2A>G XP_011532452.1:n.2081-2A>G
XM_011534151.1:c.2072-2A>G XP_011532453.1:n.2072-2A>G
XM_011534152.1:c.2012-2A>G XP_011532454.1:n.2012-2A>G
XM_011534149.3:c.2126-2A>G XP_011532451.1:n.2126-2A>G
XM_011534150.3:c.2081-2A>G XP_011532452.1:n.2081-2A>G
XM_011534151.3:c.2072-2A>G XP_011532453.1:n.2072-2A>G
XM_011534152.2:c.2012-2A>G XP_011532454.1:n.2012-2A>G
XM_017007303.2:c.2003-2A>G XP_016862792.1:n.2003-2A>G
NM_004656.4:c.2057-2A>G MANE Select NP_004647.1:n.2057-2A>G