Canonical Allele Identifier: CA353112620

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52408062A>G , CM000665.2:g.52408062A>G	GRCh38
NC_000003.11:g.52442078A>G , CM000665.1:g.52442078A>G	GRCh37
NC_000003.10:g.52417118A>G	NCBI36
NG_031859.1:g.6932T>C , LRG_529:g.6932T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.271T>C MANE Select	ENSP00000417132.1:p.Cys91Arg
ENST00000296288.9:c.271T>C	ENSP00000296288.5:p.Cys91Arg
ENST00000460680.5:c.271T>C	ENSP00000417132.1:p.Cys91Arg
ENST00000470173.1:c.34T>C	ENSP00000417776.1:p.Cys12Arg
ENST00000483984.5:n.271T>C
ENST00000490917.1:c.*12T>C	ENSP00000419709.1:n.*12T>C
NM_004656.3:c.271T>C	NP_004647.1:p.Cys91Arg
XM_011534149.1:c.271T>C	XP_011532451.1:p.Cys91Arg
XM_011534150.1:c.271T>C	XP_011532452.1:p.Cys91Arg
XM_011534151.1:c.271T>C	XP_011532453.1:p.Cys91Arg
XM_011534152.1:c.271T>C	XP_011532454.1:p.Cys91Arg
XM_011534149.3:c.271T>C	XP_011532451.1:p.Cys91Arg
XM_011534150.3:c.271T>C	XP_011532452.1:p.Cys91Arg
XM_011534151.3:c.271T>C	XP_011532453.1:p.Cys91Arg
XM_011534152.2:c.271T>C	XP_011532454.1:p.Cys91Arg
XM_017007303.2:c.271T>C	XP_016862792.1:p.Cys91Arg
NM_004656.4:c.271T>C MANE Select	NP_004647.1:p.Cys91Arg