Canonical Allele Identifier: CA353101538

Gene: BAP1

Linked Data

• ClinVar Variation Id: 2111846
• ClinVar RCV Id: RCV003024054
• MyVariant Identifiers: chr3:g.52437755C>G (hg19) ; chr3:g.52403739C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403739C>G , CM000665.2:g.52403739C>G	GRCh38
NC_000003.11:g.52437755C>G , CM000665.1:g.52437755C>G	GRCh37
NC_000003.10:g.52412795C>G	NCBI36
NG_031859.1:g.11255G>C , LRG_529:g.11255G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000460680.6:c.1406G>C MANE Select	ENSP00000417132.1:p.Ser469Thr
ENST00000296288.9:c.1352G>C	ENSP00000296288.5:p.Ser451Thr
ENST00000460680.5:c.1406G>C	ENSP00000417132.1:p.Ser469Thr
ENST00000469613.5:c.119+62G>C
ENST00000490804.1:n.834G>C
NM_004656.3:c.1406G>C	NP_004647.1:p.Ser469Thr
XM_011534149.1:c.1406G>C	XP_011532451.1:p.Ser469Thr
XM_011534150.1:c.1406G>C	XP_011532452.1:p.Ser469Thr
XM_011534151.1:c.1352G>C	XP_011532453.1:p.Ser451Thr
XM_011534152.1:c.1406G>C	XP_011532454.1:p.Ser469Thr
XM_011534149.3:c.1406G>C	XP_011532451.1:p.Ser469Thr
XM_011534150.3:c.1406G>C	XP_011532452.1:p.Ser469Thr
XM_011534151.3:c.1352G>C	XP_011532453.1:p.Ser451Thr
XM_011534152.2:c.1406G>C	XP_011532454.1:p.Ser469Thr
XM_017007303.2:c.1352G>C	XP_016862792.1:p.Ser451Thr
NM_004656.4:c.1406G>C MANE Select	NP_004647.1:p.Ser469Thr