Canonical Allele Identifier: CA353098292
Gene: BAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52403194T>A , CM000665.2:g.52403194T>A GRCh38
NC_000003.11:g.52437210T>A , CM000665.1:g.52437210T>A GRCh37
NC_000003.10:g.52412250T>A NCBI36
NG_031859.1:g.11800A>T , LRG_529:g.11800A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000460680.6:c.1834A>T MANE Select ENSP00000417132.1:p.Lys612Ter
ENST00000296288.9:c.1780A>T ENSP00000296288.5:p.Lys594Ter
ENST00000460680.5:c.1834A>T ENSP00000417132.1:p.Lys612Ter
ENST00000466093.1:n.241A>T
ENST00000469613.5:c.120-353A>T
ENST00000478368.1:c.337A>T ENSP00000420647.1:p.Lys113Ter
NM_004656.3:c.1834A>T NP_004647.1:p.Lys612Ter
XM_011534149.1:c.1834A>T XP_011532451.1:p.Lys612Ter
XM_011534150.1:c.1834A>T XP_011532452.1:p.Lys612Ter
XM_011534151.1:c.1780A>T XP_011532453.1:p.Lys594Ter
XM_011534152.1:c.1834A>T XP_011532454.1:p.Lys612Ter
XM_011534149.3:c.1834A>T XP_011532451.1:p.Lys612Ter
XM_011534150.3:c.1834A>T XP_011532452.1:p.Lys612Ter
XM_011534151.3:c.1780A>T XP_011532453.1:p.Lys594Ter
XM_011534152.2:c.1834A>T XP_011532454.1:p.Lys612Ter
XM_017007303.2:c.1780A>T XP_016862792.1:p.Lys594Ter
NM_004656.4:c.1834A>T MANE Select NP_004647.1:p.Lys612Ter