Canonical Allele Identifier: CA1925632004

Gene: LDB3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86716702_86716703delinsTC , CM000672.2:g.86716702_86716703delinsTC	GRCh38
NC_000010.10:g.88476459_88476460delinsTC , CM000672.1:g.88476459_88476460delinsTC	GRCh37
NC_000010.9:g.88466439_88466440delinsTC	NCBI36
NG_008876.1:g.53139_53140delinsTC , LRG_385:g.53139_53140delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687154.1:n.515-2025_515-2024delinsTC
ENST00000688001.1:c.1418_1419delinsTC	ENSP00000508987.1:p.Val473=
ENST00000689296.1:c.1418_1419delinsTC	ENSP00000510609.1:p.Val473=
ENST00000689740.1:c.1466_1467delinsTC	ENSP00000510300.1:p.Val489=
ENST00000693680.1:c.1466_1467delinsTC	ENSP00000509539.1:p.Val489=
ENST00000361373.9:c.1607_1608delinsTC MANE Select	ENSP00000355296.3:p.Val536=
ENST00000429277.7:c.1277_1278delinsTC	ENSP00000401437.3:p.Val426=
ENST00000623056.4:c.1622_1623delinsTC	ENSP00000485500.1:p.Val541=
ENST00000263066.10:c.1277_1278delinsTC	ENSP00000263066.6:p.Val426=
ENST00000361373.8:c.1607_1608delinsTC	ENSP00000355296.3:p.Val536=
ENST00000429277.6:c.1622_1623delinsTC	ENSP00000401437.2:p.Val541=
ENST00000623056.3:c.1622_1623delinsTC	ENSP00000485500.1:p.Val541=
NM_001080114.1:c.1277_1278delinsTC	NP_001073583.1:p.Val426=
NM_001171610.1:c.1622_1623delinsTC	NP_001165081.1:p.Val541=
NM_007078.2:c.1607_1608delinsTC , LRG_385t1:c.1607_1608delinsTC	NP_009009.1:p.Val536=
XM_005269464.3:c.1607_1608delinsTC	XP_005269521.1:p.Val536=
XM_005269466.3:c.1418_1419delinsTC	XP_005269523.1:p.Val473=
XM_011539184.1:c.1859_1860delinsTC	XP_011537486.1:p.Val620=
XM_011539185.1:c.1859_1860delinsTC	XP_011537487.1:p.Val620=
XM_011539186.1:c.1811_1812delinsTC	XP_011537488.1:p.Val604=
XM_011539187.1:c.1670_1671delinsTC	XP_011537489.1:p.Val557=
XM_011539188.1:c.1655_1656delinsTC	XP_011537490.1:p.Val552=
XM_011539189.1:c.1514_1515delinsTC	XP_011537491.1:p.Val505=
XM_011539190.1:c.1466_1467delinsTC	XP_011537492.1:p.Val489=
XM_011539191.1:c.1325_1326delinsTC	XP_011537493.1:p.Val442=
XM_011539192.1:c.1310_1311delinsTC	XP_011537494.1:p.Val437=
XM_011539193.1:c.815_816delinsTC	XP_011537495.1:p.Val272=
XM_011539194.1:c.626_627delinsTC	XP_011537496.1:p.Val209=
XM_005269464.4:c.1607_1608delinsTC	XP_005269521.1:p.Val536=
XM_005269466.4:c.1418_1419delinsTC	XP_005269523.1:p.Val473=
XM_011539184.2:c.1859_1860delinsTC	XP_011537486.1:p.Val620=
XM_011539185.2:c.1859_1860delinsTC	XP_011537487.1:p.Val620=
XM_011539186.2:c.1811_1812delinsTC	XP_011537488.1:p.Val604=
XM_011539187.2:c.1670_1671delinsTC	XP_011537489.1:p.Val557=
XM_011539188.2:c.1655_1656delinsTC	XP_011537490.1:p.Val552=
XM_011539190.2:c.1466_1467delinsTC	XP_011537492.1:p.Val489=
XM_011539191.2:c.1325_1326delinsTC	XP_011537493.1:p.Val442=
XM_017015606.1:c.1655_1656delinsTC	XP_016871095.1:p.Val552=
XM_017015607.1:c.815_816delinsTC	XP_016871096.1:p.Val272=
XM_024447785.1:c.1514_1515delinsTC	XP_024303553.1:p.Val505=
XM_024447786.1:c.1277_1278delinsTC	XP_024303554.1:p.Val426=
NM_001080114.2:c.1277_1278delinsTC	NP_001073583.1:p.Val426=
NM_001171610.2:c.1622_1623delinsTC	NP_001165081.1:p.Val541=
NM_001368064.1:c.1418_1419delinsTC	NP_001354993.1:p.Val473=
NM_001368065.1:c.1418_1419delinsTC	NP_001354994.1:p.Val473=
NM_001368066.1:c.1466_1467delinsTC	NP_001354995.1:p.Val489=
NM_007078.3:c.1607_1608delinsTC MANE Select	NP_009009.1:p.Val536=