Canonical Allele Identifier: CA1925631964
Gene: LDB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86716630A= , CM000672.2:g.86716630A= GRCh38
NC_000010.10:g.88476387A= , CM000672.1:g.88476387A= GRCh37
NC_000010.9:g.88466367A= NCBI36
NG_008876.1:g.53067A= , LRG_385:g.53067A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000687154.1:n.515-2097A=
ENST00000688001.1:c.1346A= ENSP00000508987.1:p.Gln449=
ENST00000689296.1:c.1346A= ENSP00000510609.1:p.Gln449=
ENST00000689740.1:c.1394A= ENSP00000510300.1:p.Gln465=
ENST00000693680.1:c.1394A= ENSP00000509539.1:p.Gln465=
ENST00000361373.9:c.1535A= MANE Select ENSP00000355296.3:p.Gln512=
ENST00000429277.7:c.1205A= ENSP00000401437.3:p.Gln402=
ENST00000623056.4:c.1550A= ENSP00000485500.1:p.Gln517=
ENST00000263066.10:c.1205A= ENSP00000263066.6:p.Gln402=
ENST00000361373.8:c.1535A= ENSP00000355296.3:p.Gln512=
ENST00000429277.6:c.1550A= ENSP00000401437.2:p.Gln517=
ENST00000623056.3:c.1550A= ENSP00000485500.1:p.Gln517=
NM_001080114.1:c.1205A= NP_001073583.1:p.Gln402=
NM_001171610.1:c.1550A= NP_001165081.1:p.Gln517=
NM_007078.2:c.1535A= , LRG_385t1:c.1535A= NP_009009.1:p.Gln512=
XM_005269464.3:c.1535A= XP_005269521.1:p.Gln512=
XM_005269466.3:c.1346A= XP_005269523.1:p.Gln449=
XM_011539184.1:c.1787A= XP_011537486.1:p.Gln596=
XM_011539185.1:c.1787A= XP_011537487.1:p.Gln596=
XM_011539186.1:c.1739A= XP_011537488.1:p.Gln580=
XM_011539187.1:c.1598A= XP_011537489.1:p.Gln533=
XM_011539188.1:c.1583A= XP_011537490.1:p.Gln528=
XM_011539189.1:c.1442A= XP_011537491.1:p.Gln481=
XM_011539190.1:c.1394A= XP_011537492.1:p.Gln465=
XM_011539191.1:c.1253A= XP_011537493.1:p.Gln418=
XM_011539192.1:c.1238A= XP_011537494.1:p.Gln413=
XM_011539193.1:c.743A= XP_011537495.1:p.Gln248=
XM_011539194.1:c.554A= XP_011537496.1:p.Gln185=
XM_005269464.4:c.1535A= XP_005269521.1:p.Gln512=
XM_005269466.4:c.1346A= XP_005269523.1:p.Gln449=
XM_011539184.2:c.1787A= XP_011537486.1:p.Gln596=
XM_011539185.2:c.1787A= XP_011537487.1:p.Gln596=
XM_011539186.2:c.1739A= XP_011537488.1:p.Gln580=
XM_011539187.2:c.1598A= XP_011537489.1:p.Gln533=
XM_011539188.2:c.1583A= XP_011537490.1:p.Gln528=
XM_011539190.2:c.1394A= XP_011537492.1:p.Gln465=
XM_011539191.2:c.1253A= XP_011537493.1:p.Gln418=
XM_017015606.1:c.1583A= XP_016871095.1:p.Gln528=
XM_017015607.1:c.743A= XP_016871096.1:p.Gln248=
XM_024447785.1:c.1442A= XP_024303553.1:p.Gln481=
XM_024447786.1:c.1205A= XP_024303554.1:p.Gln402=
NM_001080114.2:c.1205A= NP_001073583.1:p.Gln402=
NM_001171610.2:c.1550A= NP_001165081.1:p.Gln517=
NM_001368064.1:c.1346A= NP_001354993.1:p.Gln449=
NM_001368065.1:c.1346A= NP_001354994.1:p.Gln449=
NM_001368066.1:c.1394A= NP_001354995.1:p.Gln465=
NM_007078.3:c.1535A= MANE Select NP_009009.1:p.Gln512=