Canonical Allele Identifier: CA1364836208

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403377G= , CM000665.2:g.52403377G=	GRCh38
NC_000003.11:g.52437393G= , CM000665.1:g.52437393G=	GRCh37
NC_000003.10:g.52412433G=	NCBI36
NG_031859.1:g.11617C= , LRG_529:g.11617C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1729+39C= MANE Select	ENSP00000417132.1:n.1729+39C=
ENST00000296288.9:c.1675+39C=	ENSP00000296288.5:n.1675+39C=
ENST00000460680.5:c.1729+39C=	ENSP00000417132.1:n.1729+39C=
ENST00000466093.1:n.136+39C=
ENST00000469613.5:c.119+424C=
ENST00000478368.1:c.232+39C=	ENSP00000420647.1:n.232+39C=
NM_004656.3:c.1729+39C=	NP_004647.1:n.1729+39C=
XM_011534149.1:c.1729+39C=	XP_011532451.1:n.1729+39C=
XM_011534150.1:c.1729+39C=	XP_011532452.1:n.1729+39C=
XM_011534151.1:c.1675+39C=	XP_011532453.1:n.1675+39C=
XM_011534152.1:c.1729+39C=	XP_011532454.1:n.1729+39C=
XM_011534149.3:c.1729+39C=	XP_011532451.1:n.1729+39C=
XM_011534150.3:c.1729+39C=	XP_011532452.1:n.1729+39C=
XM_011534151.3:c.1675+39C=	XP_011532453.1:n.1675+39C=
XM_011534152.2:c.1729+39C=	XP_011532454.1:n.1729+39C=
XM_017007303.2:c.1675+39C=	XP_016862792.1:n.1675+39C=
NM_004656.4:c.1729+39C= MANE Select	NP_004647.1:n.1729+39C=