Canonical Allele Identifier: CA74740827

Gene: BAP1

Linked Data

• ClinVar Variation Id: 926819
• ClinVar RCV Id: RCV001189645
• dbSNP Id: rs946145283
• gnomAD v2: 3-52437750-C-T
• gnomAD v3: 3-52403734-C-T
• gnomAD v4: 3-52403734-C-T
• MyVariant Identifiers: chr3:g.52437750C>T (hg19) ; chr3:g.52403734C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403734C>T , CM000665.2:g.52403734C>T	GRCh38
NC_000003.11:g.52437750C>T , CM000665.1:g.52437750C>T	GRCh37
NC_000003.10:g.52412790C>T	NCBI36
NG_031859.1:g.11260G>A , LRG_529:g.11260G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000460680.6:c.1411G>A MANE Select	ENSP00000417132.1:p.Ala471Thr
ENST00000296288.9:c.1357G>A	ENSP00000296288.5:p.Ala453Thr
ENST00000460680.5:c.1411G>A	ENSP00000417132.1:p.Ala471Thr
ENST00000469613.5:c.119+67G>A
ENST00000490804.1:n.839G>A
NM_004656.3:c.1411G>A	NP_004647.1:p.Ala471Thr
XM_011534149.1:c.1411G>A	XP_011532451.1:p.Ala471Thr
XM_011534150.1:c.1411G>A	XP_011532452.1:p.Ala471Thr
XM_011534151.1:c.1357G>A	XP_011532453.1:p.Ala453Thr
XM_011534152.1:c.1411G>A	XP_011532454.1:p.Ala471Thr
XM_011534149.3:c.1411G>A	XP_011532451.1:p.Ala471Thr
XM_011534150.3:c.1411G>A	XP_011532452.1:p.Ala471Thr
XM_011534151.3:c.1357G>A	XP_011532453.1:p.Ala453Thr
XM_011534152.2:c.1411G>A	XP_011532454.1:p.Ala471Thr
XM_017007303.2:c.1357G>A	XP_016862792.1:p.Ala453Thr
NM_004656.4:c.1411G>A MANE Select	NP_004647.1:p.Ala471Thr