Canonical Allele Identifier: CA353094306

Gene: BAP1

Linked Data

• MyVariant Identifiers: chr3:g.52436383A>T (hg19) ; chr3:g.52402367A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402367A>T , CM000665.2:g.52402367A>T	GRCh38
NC_000003.11:g.52436383A>T , CM000665.1:g.52436383A>T	GRCh37
NC_000003.10:g.52411423A>T	NCBI36
NG_031859.1:g.12627T>A , LRG_529:g.12627T>A
NG_052911.1:g.91049A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2111T>A MANE Select	ENSP00000417132.1:p.Val704Asp
ENST00000296288.9:c.2057T>A	ENSP00000296288.5:p.Val686Asp
ENST00000460680.5:c.2111T>A	ENSP00000417132.1:p.Val704Asp
ENST00000466093.1:n.784T>A
ENST00000469613.5:c.310T>A
ENST00000478368.1:c.683T>A	ENSP00000420647.1:p.Val228Asp
NM_004656.3:c.2111T>A	NP_004647.1:p.Val704Asp
XM_011534149.1:c.2180T>A	XP_011532451.1:p.Val727Asp
XM_011534150.1:c.2135T>A	XP_011532452.1:p.Val712Asp
XM_011534151.1:c.2126T>A	XP_011532453.1:p.Val709Asp
XM_011534152.1:c.2066T>A	XP_011532454.1:p.Val689Asp
XM_011534149.3:c.2180T>A	XP_011532451.1:p.Val727Asp
XM_011534150.3:c.2135T>A	XP_011532452.1:p.Val712Asp
XM_011534151.3:c.2126T>A	XP_011532453.1:p.Val709Asp
XM_011534152.2:c.2066T>A	XP_011532454.1:p.Val689Asp
XM_017007303.2:c.2057T>A	XP_016862792.1:p.Val686Asp
NM_004656.4:c.2111T>A MANE Select	NP_004647.1:p.Val704Asp