Canonical Allele Identifier: CA353100913

Gene: BAP1

Linked Data

• ClinVar Variation Id: 2880400
• ClinVar RCV Id: RCV003642425
• gnomAD v4: 3-52403636-G-C
• MyVariant Identifiers: chr3:g.52437652G>C (hg19) ; chr3:g.52403636G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403636G>C , CM000665.2:g.52403636G>C	GRCh38
NC_000003.11:g.52437652G>C , CM000665.1:g.52437652G>C	GRCh37
NC_000003.10:g.52412692G>C	NCBI36
NG_031859.1:g.11358C>G , LRG_529:g.11358C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000460680.6:c.1509C>G MANE Select	ENSP00000417132.1:p.Phe503Leu
ENST00000296288.9:c.1455C>G	ENSP00000296288.5:p.Phe485Leu
ENST00000460680.5:c.1509C>G	ENSP00000417132.1:p.Phe503Leu
ENST00000469613.5:c.119+165C>G
ENST00000478368.1:c.12C>G	ENSP00000420647.1:p.Phe4Leu
NM_004656.3:c.1509C>G	NP_004647.1:p.Phe503Leu
XM_011534149.1:c.1509C>G	XP_011532451.1:p.Phe503Leu
XM_011534150.1:c.1509C>G	XP_011532452.1:p.Phe503Leu
XM_011534151.1:c.1455C>G	XP_011532453.1:p.Phe485Leu
XM_011534152.1:c.1509C>G	XP_011532454.1:p.Phe503Leu
XM_011534149.3:c.1509C>G	XP_011532451.1:p.Phe503Leu
XM_011534150.3:c.1509C>G	XP_011532452.1:p.Phe503Leu
XM_011534151.3:c.1455C>G	XP_011532453.1:p.Phe485Leu
XM_011534152.2:c.1509C>G	XP_011532454.1:p.Phe503Leu
XM_017007303.2:c.1455C>G	XP_016862792.1:p.Phe485Leu
NM_004656.4:c.1509C>G MANE Select	NP_004647.1:p.Phe503Leu