Canonical Allele Identifier: CA353094320

Gene: BAP1

Linked Data

• gnomAD v4: 3-52402371-C-T
• MyVariant Identifiers: chr3:g.52436387C>T (hg19) ; chr3:g.52402371C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402371C>T , CM000665.2:g.52402371C>T	GRCh38
NC_000003.11:g.52436387C>T , CM000665.1:g.52436387C>T	GRCh37
NC_000003.10:g.52411427C>T	NCBI36
NG_031859.1:g.12623G>A , LRG_529:g.12623G>A
NG_052911.1:g.91053C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2107G>A MANE Select	ENSP00000417132.1:p.Gly703Arg
ENST00000296288.9:c.2053G>A	ENSP00000296288.5:p.Gly685Arg
ENST00000460680.5:c.2107G>A	ENSP00000417132.1:p.Gly703Arg
ENST00000466093.1:n.780G>A
ENST00000469613.5:c.306G>A
ENST00000478368.1:c.679G>A	ENSP00000420647.1:p.Gly227Arg
NM_004656.3:c.2107G>A	NP_004647.1:p.Gly703Arg
XM_011534149.1:c.2176G>A	XP_011532451.1:p.Gly726Arg
XM_011534150.1:c.2131G>A	XP_011532452.1:p.Gly711Arg
XM_011534151.1:c.2122G>A	XP_011532453.1:p.Gly708Arg
XM_011534152.1:c.2062G>A	XP_011532454.1:p.Gly688Arg
XM_011534149.3:c.2176G>A	XP_011532451.1:p.Gly726Arg
XM_011534150.3:c.2131G>A	XP_011532452.1:p.Gly711Arg
XM_011534151.3:c.2122G>A	XP_011532453.1:p.Gly708Arg
XM_011534152.2:c.2062G>A	XP_011532454.1:p.Gly688Arg
XM_017007303.2:c.2053G>A	XP_016862792.1:p.Gly685Arg
NM_004656.4:c.2107G>A MANE Select	NP_004647.1:p.Gly703Arg