Canonical Allele Identifier: CA433886141

Gene: BAP1

Linked Data

• dbSNP Id: rs1276570098
• MyVariant Identifiers: chr3:g.52437307C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403291C>G , CM000665.2:g.52403291C>G	GRCh38
NC_000003.11:g.52437307C>G , CM000665.1:g.52437307C>G	GRCh37
NC_000003.10:g.52412347C>G	NCBI36
NG_031859.1:g.11703G>C , LRG_529:g.11703G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1737G>C MANE Select	ENSP00000417132.1:p.Gly579=
ENST00000296288.9:c.1683G>C	ENSP00000296288.5:p.Gly561=
ENST00000460680.5:c.1737G>C	ENSP00000417132.1:p.Gly579=
ENST00000466093.1:n.144G>C
ENST00000469613.5:c.120-450G>C
ENST00000478368.1:c.240G>C	ENSP00000420647.1:p.Gly80=
NM_004656.3:c.1737G>C	NP_004647.1:p.Gly579=
XM_011534149.1:c.1737G>C	XP_011532451.1:p.Gly579=
XM_011534150.1:c.1737G>C	XP_011532452.1:p.Gly579=
XM_011534151.1:c.1683G>C	XP_011532453.1:p.Gly561=
XM_011534152.1:c.1737G>C	XP_011532454.1:p.Gly579=
XM_011534149.3:c.1737G>C	XP_011532451.1:p.Gly579=
XM_011534150.3:c.1737G>C	XP_011532452.1:p.Gly579=
XM_011534151.3:c.1683G>C	XP_011532453.1:p.Gly561=
XM_011534152.2:c.1737G>C	XP_011532454.1:p.Gly579=
XM_017007303.2:c.1683G>C	XP_016862792.1:p.Gly561=
NM_004656.4:c.1737G>C MANE Select	NP_004647.1:p.Gly579=