Canonical Allele Identifier: CA1364836434

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403476T= , CM000665.2:g.52403476T=	GRCh38
NC_000003.11:g.52437492T= , CM000665.1:g.52437492T=	GRCh37
NC_000003.10:g.52412532T=	NCBI36
NG_031859.1:g.11518A= , LRG_529:g.11518A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1669A= MANE Select	ENSP00000417132.1:p.Ile557=
ENST00000296288.9:c.1615A=	ENSP00000296288.5:p.Ile539=
ENST00000460680.5:c.1669A=	ENSP00000417132.1:p.Ile557=
ENST00000466093.1:n.76A=
ENST00000469613.5:c.119+325A=
ENST00000478368.1:c.172A=	ENSP00000420647.1:p.Ile58=
NM_004656.3:c.1669A=	NP_004647.1:p.Ile557=
XM_011534149.1:c.1669A=	XP_011532451.1:p.Ile557=
XM_011534150.1:c.1669A=	XP_011532452.1:p.Ile557=
XM_011534151.1:c.1615A=	XP_011532453.1:p.Ile539=
XM_011534152.1:c.1669A=	XP_011532454.1:p.Ile557=
XM_011534149.3:c.1669A=	XP_011532451.1:p.Ile557=
XM_011534150.3:c.1669A=	XP_011532452.1:p.Ile557=
XM_011534151.3:c.1615A=	XP_011532453.1:p.Ile539=
XM_011534152.2:c.1669A=	XP_011532454.1:p.Ile557=
XM_017007303.2:c.1615A=	XP_016862792.1:p.Ile539=
NM_004656.4:c.1669A= MANE Select	NP_004647.1:p.Ile557=