Canonical Allele Identifier: CA353096189

Gene: BAP1

Linked Data

• MyVariant Identifiers: chr3:g.52436638A>C (hg19) ; chr3:g.52402622A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402622A>C , CM000665.2:g.52402622A>C	GRCh38
NC_000003.11:g.52436638A>C , CM000665.1:g.52436638A>C	GRCh37
NC_000003.10:g.52411678A>C	NCBI36
NG_031859.1:g.12372T>G , LRG_529:g.12372T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2036T>G MANE Select	ENSP00000417132.1:p.Ile679Ser
ENST00000296288.9:c.1982T>G	ENSP00000296288.5:p.Ile661Ser
ENST00000460680.5:c.2036T>G	ENSP00000417132.1:p.Ile679Ser
ENST00000466093.1:n.709T>G
ENST00000469613.5:c.235T>G
ENST00000478368.1:c.608T>G	ENSP00000420647.1:p.Ile203Ser
NM_004656.3:c.2036T>G	NP_004647.1:p.Ile679Ser
XM_011534149.1:c.2105T>G	XP_011532451.1:p.Ile702Ser
XM_011534150.1:c.2060T>G	XP_011532452.1:p.Ile687Ser
XM_011534151.1:c.2051T>G	XP_011532453.1:p.Ile684Ser
XM_011534152.1:c.1991T>G	XP_011532454.1:p.Ile664Ser
XM_011534149.3:c.2105T>G	XP_011532451.1:p.Ile702Ser
XM_011534150.3:c.2060T>G	XP_011532452.1:p.Ile687Ser
XM_011534151.3:c.2051T>G	XP_011532453.1:p.Ile684Ser
XM_011534152.2:c.1991T>G	XP_011532454.1:p.Ile664Ser
XM_017007303.2:c.1982T>G	XP_016862792.1:p.Ile661Ser
NM_004656.4:c.2036T>G MANE Select	NP_004647.1:p.Ile679Ser