Canonical Allele Identifier: CA353094486

Gene: BAP1

Linked Data

• MyVariant Identifiers: chr3:g.52436416T>C (hg19) ; chr3:g.52402400T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402400T>C , CM000665.2:g.52402400T>C	GRCh38
NC_000003.11:g.52436416T>C , CM000665.1:g.52436416T>C	GRCh37
NC_000003.10:g.52411456T>C	NCBI36
NG_031859.1:g.12594A>G , LRG_529:g.12594A>G
NG_052911.1:g.91082T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2078A>G MANE Select	ENSP00000417132.1:p.Glu693Gly
ENST00000296288.9:c.2024A>G	ENSP00000296288.5:p.Glu675Gly
ENST00000460680.5:c.2078A>G	ENSP00000417132.1:p.Glu693Gly
ENST00000466093.1:n.751A>G
ENST00000469613.5:c.277A>G
ENST00000478368.1:c.650A>G	ENSP00000420647.1:p.Glu217Gly
NM_004656.3:c.2078A>G	NP_004647.1:p.Glu693Gly
XM_011534149.1:c.2147A>G	XP_011532451.1:p.Glu716Gly
XM_011534150.1:c.2102A>G	XP_011532452.1:p.Glu701Gly
XM_011534151.1:c.2093A>G	XP_011532453.1:p.Glu698Gly
XM_011534152.1:c.2033A>G	XP_011532454.1:p.Glu678Gly
XM_011534149.3:c.2147A>G	XP_011532451.1:p.Glu716Gly
XM_011534150.3:c.2102A>G	XP_011532452.1:p.Glu701Gly
XM_011534151.3:c.2093A>G	XP_011532453.1:p.Glu698Gly
XM_011534152.2:c.2033A>G	XP_011532454.1:p.Glu678Gly
XM_017007303.2:c.2024A>G	XP_016862792.1:p.Glu675Gly
NM_004656.4:c.2078A>G MANE Select	NP_004647.1:p.Glu693Gly