Canonical Allele Identifier: CA353107671
Gene: BAP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52406378T>C , CM000665.2:g.52406378T>C GRCh38
NC_000003.11:g.52440394T>C , CM000665.1:g.52440394T>C GRCh37
NC_000003.10:g.52415434T>C NCBI36
NG_031859.1:g.8616A>G , LRG_529:g.8616A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000460680.6:c.660-2A>G MANE Select ENSP00000417132.1:n.660-2A>G
ENST00000296288.9:c.660-56A>G ENSP00000296288.5:n.660-56A>G
ENST00000460680.5:c.660-2A>G ENSP00000417132.1:n.660-2A>G
ENST00000471532.5:n.825A>G
NM_004656.3:c.660-2A>G NP_004647.1:n.660-2A>G
XM_011534149.1:c.660-2A>G XP_011532451.1:n.660-2A>G
XM_011534150.1:c.660-2A>G XP_011532452.1:n.660-2A>G
XM_011534151.1:c.660-56A>G XP_011532453.1:n.660-56A>G
XM_011534152.1:c.660-2A>G XP_011532454.1:n.660-2A>G
XM_011534149.3:c.660-2A>G XP_011532451.1:n.660-2A>G
XM_011534150.3:c.660-2A>G XP_011532452.1:n.660-2A>G
XM_011534151.3:c.660-56A>G XP_011532453.1:n.660-56A>G
XM_011534152.2:c.660-2A>G XP_011532454.1:n.660-2A>G
XM_017007303.2:c.660-56A>G XP_016862792.1:n.660-56A>G
NM_004656.4:c.660-2A>G MANE Select NP_004647.1:n.660-2A>G
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