Canonical Allele Identifier: CA2436747

Gene: BAP1

Linked Data

• ClinVar Variation Id: 240050
• ClinVar RCV Id: RCV000225985 ; RCV000247370 ; RCV000579745 ; RCV000857988 ; RCV003316285 ; RCV002494649
• dbSNP Id: rs150945583
• ExAC: 3:52437424 A / G
• gnomAD v2: 3-52437424-A-G
• gnomAD v3: 3-52403408-A-G
• gnomAD v4: 3-52403408-A-G
• MyVariant Identifiers: chr3:g.52437424A>G (hg19) ; chr3:g.52403408A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403408A>G , CM000665.2:g.52403408A>G	GRCh38
NC_000003.11:g.52437424A>G , CM000665.1:g.52437424A>G	GRCh37
NC_000003.10:g.52412464A>G	NCBI36
NG_031859.1:g.11586T>C , LRG_529:g.11586T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1729+8T>C MANE Select	ENSP00000417132.1:n.1729+8T>C
ENST00000296288.9:c.1675+8T>C	ENSP00000296288.5:n.1675+8T>C
ENST00000460680.5:c.1729+8T>C	ENSP00000417132.1:n.1729+8T>C
ENST00000466093.1:n.136+8T>C
ENST00000469613.5:c.119+393T>C
ENST00000478368.1:c.232+8T>C	ENSP00000420647.1:n.232+8T>C
NM_004656.3:c.1729+8T>C	NP_004647.1:n.1729+8T>C
XM_011534149.1:c.1729+8T>C	XP_011532451.1:n.1729+8T>C
XM_011534150.1:c.1729+8T>C	XP_011532452.1:n.1729+8T>C
XM_011534151.1:c.1675+8T>C	XP_011532453.1:n.1675+8T>C
XM_011534152.1:c.1729+8T>C	XP_011532454.1:n.1729+8T>C
XM_011534149.3:c.1729+8T>C	XP_011532451.1:n.1729+8T>C
XM_011534150.3:c.1729+8T>C	XP_011532452.1:n.1729+8T>C
XM_011534151.3:c.1675+8T>C	XP_011532453.1:n.1675+8T>C
XM_011534152.2:c.1729+8T>C	XP_011532454.1:n.1729+8T>C
XM_017007303.2:c.1675+8T>C	XP_016862792.1:n.1675+8T>C
NM_004656.4:c.1729+8T>C MANE Select	NP_004647.1:n.1729+8T>C