Canonical Allele Identifier: CA433886341

Gene: BAP1

Linked Data

• ClinVar Variation Id: 1772026
• ClinVar RCV Id: RCV002389503
• dbSNP Id: rs764923860
• MyVariant Identifiers: chr3:g.52437751C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403735C>G , CM000665.2:g.52403735C>G	GRCh38
NC_000003.11:g.52437751C>G , CM000665.1:g.52437751C>G	GRCh37
NC_000003.10:g.52412791C>G	NCBI36
NG_031859.1:g.11259G>C , LRG_529:g.11259G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000460680.6:c.1410G>C MANE Select	ENSP00000417132.1:p.Gly470=
ENST00000296288.9:c.1356G>C	ENSP00000296288.5:p.Gly452=
ENST00000460680.5:c.1410G>C	ENSP00000417132.1:p.Gly470=
ENST00000469613.5:c.119+66G>C
ENST00000490804.1:n.838G>C
NM_004656.3:c.1410G>C	NP_004647.1:p.Gly470=
XM_011534149.1:c.1410G>C	XP_011532451.1:p.Gly470=
XM_011534150.1:c.1410G>C	XP_011532452.1:p.Gly470=
XM_011534151.1:c.1356G>C	XP_011532453.1:p.Gly452=
XM_011534152.1:c.1410G>C	XP_011532454.1:p.Gly470=
XM_011534149.3:c.1410G>C	XP_011532451.1:p.Gly470=
XM_011534150.3:c.1410G>C	XP_011532452.1:p.Gly470=
XM_011534151.3:c.1356G>C	XP_011532453.1:p.Gly452=
XM_011534152.2:c.1410G>C	XP_011532454.1:p.Gly470=
XM_017007303.2:c.1356G>C	XP_016862792.1:p.Gly452=
NM_004656.4:c.1410G>C MANE Select	NP_004647.1:p.Gly470=