Canonical Allele Identifier: CA16611338

Gene: BAP1

Linked Data

• ClinVar Variation Id: 412431
• ClinVar RCV Id: RCV000469426
• dbSNP Id: rs1060503742
• MyVariant Identifiers: chr3:g.52437164T>A (hg19) ; chr3:g.52403148T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403148T>A , CM000665.2:g.52403148T>A	GRCh38
NC_000003.11:g.52437164T>A , CM000665.1:g.52437164T>A	GRCh37
NC_000003.10:g.52412204T>A	NCBI36
NG_031859.1:g.11846A>T , LRG_529:g.11846A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1880A>T MANE Select	ENSP00000417132.1:p.Tyr627Phe
ENST00000296288.9:c.1826A>T	ENSP00000296288.5:p.Tyr609Phe
ENST00000460680.5:c.1880A>T	ENSP00000417132.1:p.Tyr627Phe
ENST00000466093.1:n.287A>T
ENST00000469613.5:c.120-307A>T
ENST00000478368.1:c.383A>T	ENSP00000420647.1:p.Tyr128Phe
NM_004656.3:c.1880A>T	NP_004647.1:p.Tyr627Phe
XM_011534149.1:c.1880A>T	XP_011532451.1:p.Tyr627Phe
XM_011534150.1:c.1845+35A>T	XP_011532452.1:n.1845+35A>T
XM_011534151.1:c.1826A>T	XP_011532453.1:p.Tyr609Phe
XM_011534152.1:c.1845+35A>T	XP_011532454.1:n.1845+35A>T
XM_011534149.3:c.1880A>T	XP_011532451.1:p.Tyr627Phe
XM_011534150.3:c.1845+35A>T	XP_011532452.1:n.1845+35A>T
XM_011534151.3:c.1826A>T	XP_011532453.1:p.Tyr609Phe
XM_011534152.2:c.1845+35A>T	XP_011532454.1:n.1845+35A>T
XM_017007303.2:c.1826A>T	XP_016862792.1:p.Tyr609Phe
NM_004656.4:c.1880A>T MANE Select	NP_004647.1:p.Tyr627Phe