Canonical Allele Identifier: CA2436692

Gene: BAP1

Linked Data

• ClinVar Variation Id: 490822
• ClinVar RCV Id: RCV000581891 ; RCV002061707 ; RCV002465727
• dbSNP Id: rs537090290
• ExAC: 3:52437143 C / T
• gnomAD v2: 3-52437143-C-T
• gnomAD v3: 3-52403127-C-T
• gnomAD v4: 3-52403127-C-T
• COSMIC: COSN19728383
• MyVariant Identifiers: chr3:g.52437143C>T (hg19) ; chr3:g.52403127C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403127C>T , CM000665.2:g.52403127C>T	GRCh38
NC_000003.11:g.52437143C>T , CM000665.1:g.52437143C>T	GRCh37
NC_000003.10:g.52412183C>T	NCBI36
NG_031859.1:g.11867G>A , LRG_529:g.11867G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1890+11G>A MANE Select	ENSP00000417132.1:n.1890+11G>A
ENST00000296288.9:c.1836+11G>A	ENSP00000296288.5:n.1836+11G>A
ENST00000460680.5:c.1890+11G>A	ENSP00000417132.1:n.1890+11G>A
ENST00000466093.1:n.308G>A
ENST00000469613.5:c.120-286G>A
ENST00000478368.1:c.393+11G>A	ENSP00000420647.1:n.393+11G>A
NM_004656.3:c.1890+11G>A	NP_004647.1:n.1890+11G>A
XM_011534149.1:c.1890+11G>A	XP_011532451.1:n.1890+11G>A
XM_011534150.1:c.1845+56G>A	XP_011532452.1:n.1845+56G>A
XM_011534151.1:c.1836+11G>A	XP_011532453.1:n.1836+11G>A
XM_011534152.1:c.1845+56G>A	XP_011532454.1:n.1845+56G>A
XM_011534149.3:c.1890+11G>A	XP_011532451.1:n.1890+11G>A
XM_011534150.3:c.1845+56G>A	XP_011532452.1:n.1845+56G>A
XM_011534151.3:c.1836+11G>A	XP_011532453.1:n.1836+11G>A
XM_011534152.2:c.1845+56G>A	XP_011532454.1:n.1845+56G>A
XM_017007303.2:c.1836+11G>A	XP_016862792.1:n.1836+11G>A
NM_004656.4:c.1890+11G>A MANE Select	NP_004647.1:n.1890+11G>A