Canonical Allele Identifier: CA377451356

Gene: LDB3

Linked Data

• gnomAD v4: 10-86716669-G-A
• COSMIC: COSM5147210 ; COSM5147211
• MyVariant Identifiers: chr10:g.88476426G>A (hg19) ; chr10:g.86716669G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86716669G>A , CM000672.2:g.86716669G>A	GRCh38
NC_000010.10:g.88476426G>A , CM000672.1:g.88476426G>A	GRCh37
NC_000010.9:g.88466406G>A	NCBI36
NG_008876.1:g.53106G>A , LRG_385:g.53106G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687154.1:n.515-2058G>A
ENST00000688001.1:c.1385G>A	ENSP00000508987.1:p.Gly462Asp
ENST00000689296.1:c.1385G>A	ENSP00000510609.1:p.Gly462Asp
ENST00000689740.1:c.1433G>A	ENSP00000510300.1:p.Gly478Asp
ENST00000693680.1:c.1433G>A	ENSP00000509539.1:p.Gly478Asp
ENST00000361373.9:c.1574G>A MANE Select	ENSP00000355296.3:p.Gly525Asp
ENST00000429277.7:c.1244G>A	ENSP00000401437.3:p.Gly415Asp
ENST00000623056.4:c.1589G>A	ENSP00000485500.1:p.Gly530Asp
ENST00000263066.10:c.1244G>A	ENSP00000263066.6:p.Gly415Asp
ENST00000361373.8:c.1574G>A	ENSP00000355296.3:p.Gly525Asp
ENST00000429277.6:c.1589G>A	ENSP00000401437.2:p.Gly530Asp
ENST00000623056.3:c.1589G>A	ENSP00000485500.1:p.Gly530Asp
NM_001080114.1:c.1244G>A	NP_001073583.1:p.Gly415Asp
NM_001171610.1:c.1589G>A	NP_001165081.1:p.Gly530Asp
NM_007078.2:c.1574G>A , LRG_385t1:c.1574G>A	NP_009009.1:p.Gly525Asp
XM_005269464.3:c.1574G>A	XP_005269521.1:p.Gly525Asp
XM_005269466.3:c.1385G>A	XP_005269523.1:p.Gly462Asp
XM_011539184.1:c.1826G>A	XP_011537486.1:p.Gly609Asp
XM_011539185.1:c.1826G>A	XP_011537487.1:p.Gly609Asp
XM_011539186.1:c.1778G>A	XP_011537488.1:p.Gly593Asp
XM_011539187.1:c.1637G>A	XP_011537489.1:p.Gly546Asp
XM_011539188.1:c.1622G>A	XP_011537490.1:p.Gly541Asp
XM_011539189.1:c.1481G>A	XP_011537491.1:p.Gly494Asp
XM_011539190.1:c.1433G>A	XP_011537492.1:p.Gly478Asp
XM_011539191.1:c.1292G>A	XP_011537493.1:p.Gly431Asp
XM_011539192.1:c.1277G>A	XP_011537494.1:p.Gly426Asp
XM_011539193.1:c.782G>A	XP_011537495.1:p.Gly261Asp
XM_011539194.1:c.593G>A	XP_011537496.1:p.Gly198Asp
XM_005269464.4:c.1574G>A	XP_005269521.1:p.Gly525Asp
XM_005269466.4:c.1385G>A	XP_005269523.1:p.Gly462Asp
XM_011539184.2:c.1826G>A	XP_011537486.1:p.Gly609Asp
XM_011539185.2:c.1826G>A	XP_011537487.1:p.Gly609Asp
XM_011539186.2:c.1778G>A	XP_011537488.1:p.Gly593Asp
XM_011539187.2:c.1637G>A	XP_011537489.1:p.Gly546Asp
XM_011539188.2:c.1622G>A	XP_011537490.1:p.Gly541Asp
XM_011539190.2:c.1433G>A	XP_011537492.1:p.Gly478Asp
XM_011539191.2:c.1292G>A	XP_011537493.1:p.Gly431Asp
XM_017015606.1:c.1622G>A	XP_016871095.1:p.Gly541Asp
XM_017015607.1:c.782G>A	XP_016871096.1:p.Gly261Asp
XM_024447785.1:c.1481G>A	XP_024303553.1:p.Gly494Asp
XM_024447786.1:c.1244G>A	XP_024303554.1:p.Gly415Asp
NM_001080114.2:c.1244G>A	NP_001073583.1:p.Gly415Asp
NM_001171610.2:c.1589G>A	NP_001165081.1:p.Gly530Asp
NM_001368064.1:c.1385G>A	NP_001354993.1:p.Gly462Asp
NM_001368065.1:c.1385G>A	NP_001354994.1:p.Gly462Asp
NM_001368066.1:c.1433G>A	NP_001354995.1:p.Gly478Asp
NM_007078.3:c.1574G>A MANE Select	NP_009009.1:p.Gly525Asp