Canonical Allele Identifier: CA1364836269

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403414_52403415delinsAC , CM000665.2:g.52403414_52403415delinsAC	GRCh38
NC_000003.11:g.52437430_52437431delinsAC , CM000665.1:g.52437430_52437431delinsAC	GRCh37
NC_000003.10:g.52412470_52412471delinsAC	NCBI36
NG_031859.1:g.11579_11580delinsGT , LRG_529:g.11579_11580delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1729+1_1729+2delinsGT MANE Select	ENSP00000417132.1:n.1729+1_1729+2delinsGT
ENST00000296288.9:c.1675+1_1675+2delinsGT	ENSP00000296288.5:n.1675+1_1675+2delinsGT
ENST00000460680.5:c.1729+1_1729+2delinsGT	ENSP00000417132.1:n.1729+1_1729+2delinsGT
ENST00000466093.1:n.136+1_136+2delinsGT
ENST00000469613.5:c.119+386_119+387delinsGT
ENST00000478368.1:c.232+1_232+2delinsGT	ENSP00000420647.1:n.232+1_232+2delinsGT
NM_004656.3:c.1729+1_1729+2delinsGT	NP_004647.1:n.1729+1_1729+2delinsGT
XM_011534149.1:c.1729+1_1729+2delinsGT	XP_011532451.1:n.1729+1_1729+2delinsGT
XM_011534150.1:c.1729+1_1729+2delinsGT	XP_011532452.1:n.1729+1_1729+2delinsGT
XM_011534151.1:c.1675+1_1675+2delinsGT	XP_011532453.1:n.1675+1_1675+2delinsGT
XM_011534152.1:c.1729+1_1729+2delinsGT	XP_011532454.1:n.1729+1_1729+2delinsGT
XM_011534149.3:c.1729+1_1729+2delinsGT	XP_011532451.1:n.1729+1_1729+2delinsGT
XM_011534150.3:c.1729+1_1729+2delinsGT	XP_011532452.1:n.1729+1_1729+2delinsGT
XM_011534151.3:c.1675+1_1675+2delinsGT	XP_011532453.1:n.1675+1_1675+2delinsGT
XM_011534152.2:c.1729+1_1729+2delinsGT	XP_011532454.1:n.1729+1_1729+2delinsGT
XM_017007303.2:c.1675+1_1675+2delinsGT	XP_016862792.1:n.1675+1_1675+2delinsGT
NM_004656.4:c.1729+1_1729+2delinsGT MANE Select	NP_004647.1:n.1729+1_1729+2delinsGT