Canonical Allele Identifier: CA433885780
Gene: BAP1 HGNC NCBI

Linked Data

dbSNP Id: rs1705036297
MyVariant Identifiers: chr3:g.52437451C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52403435C>A , CM000665.2:g.52403435C>A GRCh38
NC_000003.11:g.52437451C>A , CM000665.1:g.52437451C>A GRCh37
NC_000003.10:g.52412491C>A NCBI36
NG_031859.1:g.11559G>T , LRG_529:g.11559G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000460680.6:c.1710G>T MANE Select ENSP00000417132.1:p.Leu570=
ENST00000296288.9:c.1656G>T ENSP00000296288.5:p.Leu552=
ENST00000460680.5:c.1710G>T ENSP00000417132.1:p.Leu570=
ENST00000466093.1:n.117G>T
ENST00000469613.5:c.119+366G>T
ENST00000478368.1:c.213G>T ENSP00000420647.1:p.Leu71=
NM_004656.3:c.1710G>T NP_004647.1:p.Leu570=
XM_011534149.1:c.1710G>T XP_011532451.1:p.Leu570=
XM_011534150.1:c.1710G>T XP_011532452.1:p.Leu570=
XM_011534151.1:c.1656G>T XP_011532453.1:p.Leu552=
XM_011534152.1:c.1710G>T XP_011532454.1:p.Leu570=
XM_011534149.3:c.1710G>T XP_011532451.1:p.Leu570=
XM_011534150.3:c.1710G>T XP_011532452.1:p.Leu570=
XM_011534151.3:c.1656G>T XP_011532453.1:p.Leu552=
XM_011534152.2:c.1710G>T XP_011532454.1:p.Leu570=
XM_017007303.2:c.1656G>T XP_016862792.1:p.Leu552=
NM_004656.4:c.1710G>T MANE Select NP_004647.1:p.Leu570=