Canonical Allele Identifier: CA353096218

Gene: BAP1

Linked Data

• dbSNP Id: rs2153226193
• MyVariant Identifiers: chr3:g.52436645T>A (hg19) ; chr3:g.52402629T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402629T>A , CM000665.2:g.52402629T>A	GRCh38
NC_000003.11:g.52436645T>A , CM000665.1:g.52436645T>A	GRCh37
NC_000003.10:g.52411685T>A	NCBI36
NG_031859.1:g.12365A>T , LRG_529:g.12365A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2029A>T MANE Select	ENSP00000417132.1:p.Thr677Ser
ENST00000296288.9:c.1975A>T	ENSP00000296288.5:p.Thr659Ser
ENST00000460680.5:c.2029A>T	ENSP00000417132.1:p.Thr677Ser
ENST00000466093.1:n.702A>T
ENST00000469613.5:c.228A>T
ENST00000478368.1:c.601A>T	ENSP00000420647.1:p.Thr201Ser
NM_004656.3:c.2029A>T	NP_004647.1:p.Thr677Ser
XM_011534149.1:c.2098A>T	XP_011532451.1:p.Thr700Ser
XM_011534150.1:c.2053A>T	XP_011532452.1:p.Thr685Ser
XM_011534151.1:c.2044A>T	XP_011532453.1:p.Thr682Ser
XM_011534152.1:c.1984A>T	XP_011532454.1:p.Thr662Ser
XM_011534149.3:c.2098A>T	XP_011532451.1:p.Thr700Ser
XM_011534150.3:c.2053A>T	XP_011532452.1:p.Thr685Ser
XM_011534151.3:c.2044A>T	XP_011532453.1:p.Thr682Ser
XM_011534152.2:c.1984A>T	XP_011532454.1:p.Thr662Ser
XM_017007303.2:c.1975A>T	XP_016862792.1:p.Thr659Ser
NM_004656.4:c.2029A>T MANE Select	NP_004647.1:p.Thr677Ser