Canonical Allele Identifier: CA353096338

Gene: BAP1

Linked Data

• dbSNP Id: rs2153226218
• MyVariant Identifiers: chr3:g.52436674C>A (hg19) ; chr3:g.52402658C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402658C>A , CM000665.2:g.52402658C>A	GRCh38
NC_000003.11:g.52436674C>A , CM000665.1:g.52436674C>A	GRCh37
NC_000003.10:g.52411714C>A	NCBI36
NG_031859.1:g.12336G>T , LRG_529:g.12336G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2000G>T MANE Select	ENSP00000417132.1:p.Arg667Met
ENST00000296288.9:c.1946G>T	ENSP00000296288.5:p.Arg649Met
ENST00000460680.5:c.2000G>T	ENSP00000417132.1:p.Arg667Met
ENST00000466093.1:n.673G>T
ENST00000469613.5:c.199G>T
ENST00000478368.1:c.572G>T	ENSP00000420647.1:p.Arg191Met
NM_004656.3:c.2000G>T	NP_004647.1:p.Arg667Met
XM_011534149.1:c.2069G>T	XP_011532451.1:p.Arg690Met
XM_011534150.1:c.2024G>T	XP_011532452.1:p.Arg675Met
XM_011534151.1:c.2015G>T	XP_011532453.1:p.Arg672Met
XM_011534152.1:c.1955G>T	XP_011532454.1:p.Arg652Met
XM_011534149.3:c.2069G>T	XP_011532451.1:p.Arg690Met
XM_011534150.3:c.2024G>T	XP_011532452.1:p.Arg675Met
XM_011534151.3:c.2015G>T	XP_011532453.1:p.Arg672Met
XM_011534152.2:c.1955G>T	XP_011532454.1:p.Arg652Met
XM_017007303.2:c.1946G>T	XP_016862792.1:p.Arg649Met
NM_004656.4:c.2000G>T MANE Select	NP_004647.1:p.Arg667Met