Canonical Allele Identifier: CA1364835810

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403224_52403227delinsCCTT , CM000665.2:g.52403224_52403227delinsCCTT	GRCh38
NC_000003.11:g.52437240_52437243delinsCCTT , CM000665.1:g.52437240_52437243delinsCCTT	GRCh37
NC_000003.10:g.52412280_52412283delinsCCTT	NCBI36
NG_031859.1:g.11767_11770delinsAAGG , LRG_529:g.11767_11770delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1801_1804delinsAAGG MANE Select	ENSP00000417132.1:p.Lys601=
ENST00000296288.9:c.1747_1750delinsAAGG	ENSP00000296288.5:p.Lys583=
ENST00000460680.5:c.1801_1804delinsAAGG	ENSP00000417132.1:p.Lys601=
ENST00000466093.1:n.208_211delinsAAGG
ENST00000469613.5:c.120-386_120-383delinsAAGG
ENST00000478368.1:c.304_307delinsAAGG	ENSP00000420647.1:p.Lys102=
NM_004656.3:c.1801_1804delinsAAGG	NP_004647.1:p.Lys601=
XM_011534149.1:c.1801_1804delinsAAGG	XP_011532451.1:p.Lys601=
XM_011534150.1:c.1801_1804delinsAAGG	XP_011532452.1:p.Lys601=
XM_011534151.1:c.1747_1750delinsAAGG	XP_011532453.1:p.Lys583=
XM_011534152.1:c.1801_1804delinsAAGG	XP_011532454.1:p.Lys601=
XM_011534149.3:c.1801_1804delinsAAGG	XP_011532451.1:p.Lys601=
XM_011534150.3:c.1801_1804delinsAAGG	XP_011532452.1:p.Lys601=
XM_011534151.3:c.1747_1750delinsAAGG	XP_011532453.1:p.Lys583=
XM_011534152.2:c.1801_1804delinsAAGG	XP_011532454.1:p.Lys601=
XM_017007303.2:c.1747_1750delinsAAGG	XP_016862792.1:p.Lys583=
NM_004656.4:c.1801_1804delinsAAGG MANE Select	NP_004647.1:p.Lys601=