Canonical Allele Identifier: CA1925631871

Gene: LDB3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86716452T= , CM000672.2:g.86716452T=	GRCh38
NC_000010.10:g.88476209T= , CM000672.1:g.88476209T=	GRCh37
NC_000010.9:g.88466189T=	NCBI36
NG_008876.1:g.52889T= , LRG_385:g.52889T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687154.1:n.515-2275T=
ENST00000688001.1:c.1168T=	ENSP00000508987.1:p.Tyr390=
ENST00000689296.1:c.1168T=	ENSP00000510609.1:p.Tyr390=
ENST00000689740.1:c.1216T=	ENSP00000510300.1:p.Tyr406=
ENST00000693680.1:c.1216T=	ENSP00000509539.1:p.Tyr406=
ENST00000361373.9:c.1357T= MANE Select	ENSP00000355296.3:p.Tyr453=
ENST00000429277.7:c.1027T=	ENSP00000401437.3:p.Tyr343=
ENST00000623056.4:c.1372T=	ENSP00000485500.1:p.Tyr458=
ENST00000263066.10:c.1027T=	ENSP00000263066.6:p.Tyr343=
ENST00000361373.8:c.1357T=	ENSP00000355296.3:p.Tyr453=
ENST00000429277.6:c.1372T=	ENSP00000401437.2:p.Tyr458=
ENST00000623056.3:c.1372T=	ENSP00000485500.1:p.Tyr458=
NM_001080114.1:c.1027T=	NP_001073583.1:p.Tyr343=
NM_001171610.1:c.1372T=	NP_001165081.1:p.Tyr458=
NM_007078.2:c.1357T= , LRG_385t1:c.1357T=	NP_009009.1:p.Tyr453=
XM_005269464.3:c.1357T=	XP_005269521.1:p.Tyr453=
XM_005269466.3:c.1168T=	XP_005269523.1:p.Tyr390=
XM_011539184.1:c.1609T=	XP_011537486.1:p.Tyr537=
XM_011539185.1:c.1609T=	XP_011537487.1:p.Tyr537=
XM_011539186.1:c.1561T=	XP_011537488.1:p.Tyr521=
XM_011539187.1:c.1420T=	XP_011537489.1:p.Tyr474=
XM_011539188.1:c.1405T=	XP_011537490.1:p.Tyr469=
XM_011539189.1:c.1264T=	XP_011537491.1:p.Tyr422=
XM_011539190.1:c.1216T=	XP_011537492.1:p.Tyr406=
XM_011539191.1:c.1075T=	XP_011537493.1:p.Tyr359=
XM_011539192.1:c.1060T=	XP_011537494.1:p.Tyr354=
XM_011539193.1:c.565T=	XP_011537495.1:p.Tyr189=
XM_011539194.1:c.376T=	XP_011537496.1:p.Tyr126=
XM_005269464.4:c.1357T=	XP_005269521.1:p.Tyr453=
XM_005269466.4:c.1168T=	XP_005269523.1:p.Tyr390=
XM_011539184.2:c.1609T=	XP_011537486.1:p.Tyr537=
XM_011539185.2:c.1609T=	XP_011537487.1:p.Tyr537=
XM_011539186.2:c.1561T=	XP_011537488.1:p.Tyr521=
XM_011539187.2:c.1420T=	XP_011537489.1:p.Tyr474=
XM_011539188.2:c.1405T=	XP_011537490.1:p.Tyr469=
XM_011539190.2:c.1216T=	XP_011537492.1:p.Tyr406=
XM_011539191.2:c.1075T=	XP_011537493.1:p.Tyr359=
XM_017015606.1:c.1405T=	XP_016871095.1:p.Tyr469=
XM_017015607.1:c.565T=	XP_016871096.1:p.Tyr189=
XM_024447785.1:c.1264T=	XP_024303553.1:p.Tyr422=
XM_024447786.1:c.1027T=	XP_024303554.1:p.Tyr343=
NM_001080114.2:c.1027T=	NP_001073583.1:p.Tyr343=
NM_001171610.2:c.1372T=	NP_001165081.1:p.Tyr458=
NM_001368064.1:c.1168T=	NP_001354993.1:p.Tyr390=
NM_001368065.1:c.1168T=	NP_001354994.1:p.Tyr390=
NM_001368066.1:c.1216T=	NP_001354995.1:p.Tyr406=
NM_007078.3:c.1357T= MANE Select	NP_009009.1:p.Tyr453=