Canonical Allele Identifier: CA353099696

Gene: BAP1

Linked Data

• ClinVar Variation Id: 1041279
• ClinVar RCV Id: RCV001345060
• dbSNP Id: rs1705036790
• MyVariant Identifiers: chr3:g.52437458C>G (hg19) ; chr3:g.52403442C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403442C>G , CM000665.2:g.52403442C>G	GRCh38
NC_000003.11:g.52437458C>G , CM000665.1:g.52437458C>G	GRCh37
NC_000003.10:g.52412498C>G	NCBI36
NG_031859.1:g.11552G>C , LRG_529:g.11552G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1703G>C MANE Select	ENSP00000417132.1:p.Gly568Ala
ENST00000296288.9:c.1649G>C	ENSP00000296288.5:p.Gly550Ala
ENST00000460680.5:c.1703G>C	ENSP00000417132.1:p.Gly568Ala
ENST00000466093.1:n.110G>C
ENST00000469613.5:c.119+359G>C
ENST00000478368.1:c.206G>C	ENSP00000420647.1:p.Gly69Ala
NM_004656.3:c.1703G>C	NP_004647.1:p.Gly568Ala
XM_011534149.1:c.1703G>C	XP_011532451.1:p.Gly568Ala
XM_011534150.1:c.1703G>C	XP_011532452.1:p.Gly568Ala
XM_011534151.1:c.1649G>C	XP_011532453.1:p.Gly550Ala
XM_011534152.1:c.1703G>C	XP_011532454.1:p.Gly568Ala
XM_011534149.3:c.1703G>C	XP_011532451.1:p.Gly568Ala
XM_011534150.3:c.1703G>C	XP_011532452.1:p.Gly568Ala
XM_011534151.3:c.1649G>C	XP_011532453.1:p.Gly550Ala
XM_011534152.2:c.1703G>C	XP_011532454.1:p.Gly568Ala
XM_017007303.2:c.1649G>C	XP_016862792.1:p.Gly550Ala
NM_004656.4:c.1703G>C MANE Select	NP_004647.1:p.Gly568Ala