Canonical Allele Identifier: CA353101485

Gene: BAP1

Linked Data

• MyVariant Identifiers: chr3:g.52437747C>A (hg19) ; chr3:g.52403731C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403731C>A , CM000665.2:g.52403731C>A	GRCh38
NC_000003.11:g.52437747C>A , CM000665.1:g.52437747C>A	GRCh37
NC_000003.10:g.52412787C>A	NCBI36
NG_031859.1:g.11263G>T , LRG_529:g.11263G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000460680.6:c.1414G>T MANE Select	ENSP00000417132.1:p.Gly472Trp
ENST00000296288.9:c.1360G>T	ENSP00000296288.5:p.Gly454Trp
ENST00000460680.5:c.1414G>T	ENSP00000417132.1:p.Gly472Trp
ENST00000469613.5:c.119+70G>T
ENST00000490804.1:n.842G>T
NM_004656.3:c.1414G>T	NP_004647.1:p.Gly472Trp
XM_011534149.1:c.1414G>T	XP_011532451.1:p.Gly472Trp
XM_011534150.1:c.1414G>T	XP_011532452.1:p.Gly472Trp
XM_011534151.1:c.1360G>T	XP_011532453.1:p.Gly454Trp
XM_011534152.1:c.1414G>T	XP_011532454.1:p.Gly472Trp
XM_011534149.3:c.1414G>T	XP_011532451.1:p.Gly472Trp
XM_011534150.3:c.1414G>T	XP_011532452.1:p.Gly472Trp
XM_011534151.3:c.1360G>T	XP_011532453.1:p.Gly454Trp
XM_011534152.2:c.1414G>T	XP_011532454.1:p.Gly472Trp
XM_017007303.2:c.1360G>T	XP_016862792.1:p.Gly454Trp
NM_004656.4:c.1414G>T MANE Select	NP_004647.1:p.Gly472Trp