Canonical Allele Identifier: CA433885715

Gene: BAP1

Linked Data

• dbSNP Id: rs2153226214
• MyVariant Identifiers: chr3:g.52436670G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402654G>C , CM000665.2:g.52402654G>C	GRCh38
NC_000003.11:g.52436670G>C , CM000665.1:g.52436670G>C	GRCh37
NC_000003.10:g.52411710G>C	NCBI36
NG_031859.1:g.12340C>G , LRG_529:g.12340C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2004C>G MANE Select	ENSP00000417132.1:p.Thr668=
ENST00000296288.9:c.1950C>G	ENSP00000296288.5:p.Thr650=
ENST00000460680.5:c.2004C>G	ENSP00000417132.1:p.Thr668=
ENST00000466093.1:n.677C>G
ENST00000469613.5:c.203C>G
ENST00000478368.1:c.576C>G	ENSP00000420647.1:p.Thr192=
NM_004656.3:c.2004C>G	NP_004647.1:p.Thr668=
XM_011534149.1:c.2073C>G	XP_011532451.1:p.Thr691=
XM_011534150.1:c.2028C>G	XP_011532452.1:p.Thr676=
XM_011534151.1:c.2019C>G	XP_011532453.1:p.Thr673=
XM_011534152.1:c.1959C>G	XP_011532454.1:p.Thr653=
XM_011534149.3:c.2073C>G	XP_011532451.1:p.Thr691=
XM_011534150.3:c.2028C>G	XP_011532452.1:p.Thr676=
XM_011534151.3:c.2019C>G	XP_011532453.1:p.Thr673=
XM_011534152.2:c.1959C>G	XP_011532454.1:p.Thr653=
XM_017007303.2:c.1950C>G	XP_016862792.1:p.Thr650=
NM_004656.4:c.2004C>G MANE Select	NP_004647.1:p.Thr668=