Canonical Allele Identifier: CA377451906

Gene: LDB3

Linked Data

• MyVariant Identifiers: chr10:g.88477755C>G (hg19) ; chr10:g.86717998C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86717998C>G , CM000672.2:g.86717998C>G	GRCh38
NC_000010.10:g.88477755C>G , CM000672.1:g.88477755C>G	GRCh37
NC_000010.9:g.88467735C>G	NCBI36
NG_008876.1:g.54435C>G , LRG_385:g.54435C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000687154.1:n.515-729C>G
ENST00000688001.1:c.1522C>G	ENSP00000508987.1:p.His508Asp
ENST00000689296.1:c.1522C>G	ENSP00000510609.1:p.His508Asp
ENST00000689740.1:c.1570C>G	ENSP00000510300.1:p.His524Asp
ENST00000693680.1:c.1570C>G	ENSP00000509539.1:p.His524Asp
ENST00000361373.9:c.1711C>G MANE Select	ENSP00000355296.3:p.His571Asp
ENST00000429277.7:c.1381C>G	ENSP00000401437.3:p.His461Asp
ENST00000623056.4:c.1726C>G	ENSP00000485500.1:p.His576Asp
ENST00000263066.10:c.1381C>G	ENSP00000263066.6:p.His461Asp
ENST00000361373.8:c.1711C>G	ENSP00000355296.3:p.His571Asp
ENST00000429277.6:c.1726C>G	ENSP00000401437.2:p.His576Asp
ENST00000623056.3:c.1726C>G	ENSP00000485500.1:p.His576Asp
NM_001080114.1:c.1381C>G	NP_001073583.1:p.His461Asp
NM_001171610.1:c.1726C>G	NP_001165081.1:p.His576Asp
NM_007078.2:c.1711C>G , LRG_385t1:c.1711C>G	NP_009009.1:p.His571Asp
XM_005269464.3:c.1711C>G	XP_005269521.1:p.His571Asp
XM_005269466.3:c.1522C>G	XP_005269523.1:p.His508Asp
XM_011539184.1:c.1963C>G	XP_011537486.1:p.His655Asp
XM_011539185.1:c.1963C>G	XP_011537487.1:p.His655Asp
XM_011539186.1:c.1915C>G	XP_011537488.1:p.His639Asp
XM_011539187.1:c.1774C>G	XP_011537489.1:p.His592Asp
XM_011539188.1:c.1759C>G	XP_011537490.1:p.His587Asp
XM_011539189.1:c.1618C>G	XP_011537491.1:p.His540Asp
XM_011539190.1:c.1570C>G	XP_011537492.1:p.His524Asp
XM_011539191.1:c.1429C>G	XP_011537493.1:p.His477Asp
XM_011539192.1:c.1414C>G	XP_011537494.1:p.His472Asp
XM_011539193.1:c.919C>G	XP_011537495.1:p.His307Asp
XM_011539194.1:c.730C>G	XP_011537496.1:p.His244Asp
XM_005269464.4:c.1711C>G	XP_005269521.1:p.His571Asp
XM_005269466.4:c.1522C>G	XP_005269523.1:p.His508Asp
XM_011539184.2:c.1963C>G	XP_011537486.1:p.His655Asp
XM_011539185.2:c.1963C>G	XP_011537487.1:p.His655Asp
XM_011539186.2:c.1915C>G	XP_011537488.1:p.His639Asp
XM_011539187.2:c.1774C>G	XP_011537489.1:p.His592Asp
XM_011539188.2:c.1759C>G	XP_011537490.1:p.His587Asp
XM_011539190.2:c.1570C>G	XP_011537492.1:p.His524Asp
XM_011539191.2:c.1429C>G	XP_011537493.1:p.His477Asp
XM_017015606.1:c.1759C>G	XP_016871095.1:p.His587Asp
XM_017015607.1:c.919C>G	XP_016871096.1:p.His307Asp
XM_024447785.1:c.1618C>G	XP_024303553.1:p.His540Asp
XM_024447786.1:c.1381C>G	XP_024303554.1:p.His461Asp
NM_001080114.2:c.1381C>G	NP_001073583.1:p.His461Asp
NM_001171610.2:c.1726C>G	NP_001165081.1:p.His576Asp
NM_001368064.1:c.1522C>G	NP_001354993.1:p.His508Asp
NM_001368065.1:c.1522C>G	NP_001354994.1:p.His508Asp
NM_001368066.1:c.1570C>G	NP_001354995.1:p.His524Asp
NM_007078.3:c.1711C>G MANE Select	NP_009009.1:p.His571Asp