Canonical Allele Identifier: CA377451079

Gene: LDB3

Linked Data

• ClinVar Variation Id: 2449068
• ClinVar RCV Id: RCV003186857
• gnomAD v4: 10-86716602-G-A
• MyVariant Identifiers: chr10:g.88476359G>A (hg19) ; chr10:g.86716602G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86716602G>A , CM000672.2:g.86716602G>A	GRCh38
NC_000010.10:g.88476359G>A , CM000672.1:g.88476359G>A	GRCh37
NC_000010.9:g.88466339G>A	NCBI36
NG_008876.1:g.53039G>A , LRG_385:g.53039G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687154.1:n.515-2125G>A
ENST00000688001.1:c.1318G>A	ENSP00000508987.1:p.Gly440Ser
ENST00000689296.1:c.1318G>A	ENSP00000510609.1:p.Gly440Ser
ENST00000689740.1:c.1366G>A	ENSP00000510300.1:p.Gly456Ser
ENST00000693680.1:c.1366G>A	ENSP00000509539.1:p.Gly456Ser
ENST00000361373.9:c.1507G>A MANE Select	ENSP00000355296.3:p.Gly503Ser
ENST00000429277.7:c.1177G>A	ENSP00000401437.3:p.Gly393Ser
ENST00000623056.4:c.1522G>A	ENSP00000485500.1:p.Gly508Ser
ENST00000263066.10:c.1177G>A	ENSP00000263066.6:p.Gly393Ser
ENST00000361373.8:c.1507G>A	ENSP00000355296.3:p.Gly503Ser
ENST00000429277.6:c.1522G>A	ENSP00000401437.2:p.Gly508Ser
ENST00000623056.3:c.1522G>A	ENSP00000485500.1:p.Gly508Ser
NM_001080114.1:c.1177G>A	NP_001073583.1:p.Gly393Ser
NM_001171610.1:c.1522G>A	NP_001165081.1:p.Gly508Ser
NM_007078.2:c.1507G>A , LRG_385t1:c.1507G>A	NP_009009.1:p.Gly503Ser
XM_005269464.3:c.1507G>A	XP_005269521.1:p.Gly503Ser
XM_005269466.3:c.1318G>A	XP_005269523.1:p.Gly440Ser
XM_011539184.1:c.1759G>A	XP_011537486.1:p.Gly587Ser
XM_011539185.1:c.1759G>A	XP_011537487.1:p.Gly587Ser
XM_011539186.1:c.1711G>A	XP_011537488.1:p.Gly571Ser
XM_011539187.1:c.1570G>A	XP_011537489.1:p.Gly524Ser
XM_011539188.1:c.1555G>A	XP_011537490.1:p.Gly519Ser
XM_011539189.1:c.1414G>A	XP_011537491.1:p.Gly472Ser
XM_011539190.1:c.1366G>A	XP_011537492.1:p.Gly456Ser
XM_011539191.1:c.1225G>A	XP_011537493.1:p.Gly409Ser
XM_011539192.1:c.1210G>A	XP_011537494.1:p.Gly404Ser
XM_011539193.1:c.715G>A	XP_011537495.1:p.Gly239Ser
XM_011539194.1:c.526G>A	XP_011537496.1:p.Gly176Ser
XM_005269464.4:c.1507G>A	XP_005269521.1:p.Gly503Ser
XM_005269466.4:c.1318G>A	XP_005269523.1:p.Gly440Ser
XM_011539184.2:c.1759G>A	XP_011537486.1:p.Gly587Ser
XM_011539185.2:c.1759G>A	XP_011537487.1:p.Gly587Ser
XM_011539186.2:c.1711G>A	XP_011537488.1:p.Gly571Ser
XM_011539187.2:c.1570G>A	XP_011537489.1:p.Gly524Ser
XM_011539188.2:c.1555G>A	XP_011537490.1:p.Gly519Ser
XM_011539190.2:c.1366G>A	XP_011537492.1:p.Gly456Ser
XM_011539191.2:c.1225G>A	XP_011537493.1:p.Gly409Ser
XM_017015606.1:c.1555G>A	XP_016871095.1:p.Gly519Ser
XM_017015607.1:c.715G>A	XP_016871096.1:p.Gly239Ser
XM_024447785.1:c.1414G>A	XP_024303553.1:p.Gly472Ser
XM_024447786.1:c.1177G>A	XP_024303554.1:p.Gly393Ser
NM_001080114.2:c.1177G>A	NP_001073583.1:p.Gly393Ser
NM_001171610.2:c.1522G>A	NP_001165081.1:p.Gly508Ser
NM_001368064.1:c.1318G>A	NP_001354993.1:p.Gly440Ser
NM_001368065.1:c.1318G>A	NP_001354994.1:p.Gly440Ser
NM_001368066.1:c.1366G>A	NP_001354995.1:p.Gly456Ser
NM_007078.3:c.1507G>A MANE Select	NP_009009.1:p.Gly503Ser