Canonical Allele Identifier: CA2574457189

Gene: LDB3

Linked Data

• gnomAD v4: 10-86717894-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86717894G>T , CM000672.2:g.86717894G>T	GRCh38
NC_000010.10:g.88477651G>T , CM000672.1:g.88477651G>T	GRCh37
NC_000010.9:g.88467631G>T	NCBI36
NG_008876.1:g.54331G>T , LRG_385:g.54331G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000687154.1:n.515-833G>T
ENST00000688001.1:c.1488-70G>T	ENSP00000508987.1:n.1488-70G>T
ENST00000689296.1:c.1488-70G>T	ENSP00000510609.1:n.1488-70G>T
ENST00000689740.1:c.1536-70G>T	ENSP00000510300.1:n.1536-70G>T
ENST00000693680.1:c.1536-70G>T	ENSP00000509539.1:n.1536-70G>T
ENST00000361373.9:c.1677-70G>T MANE Select	ENSP00000355296.3:n.1677-70G>T
ENST00000429277.7:c.1347-70G>T	ENSP00000401437.3:n.1347-70G>T
ENST00000623056.4:c.1692-70G>T	ENSP00000485500.1:n.1692-70G>T
ENST00000263066.10:c.1347-70G>T	ENSP00000263066.6:n.1347-70G>T
ENST00000361373.8:c.1677-70G>T	ENSP00000355296.3:n.1677-70G>T
ENST00000429277.6:c.1692-70G>T	ENSP00000401437.2:n.1692-70G>T
ENST00000623056.3:c.1692-70G>T	ENSP00000485500.1:n.1692-70G>T
NM_001080114.1:c.1347-70G>T	NP_001073583.1:n.1347-70G>T
NM_001171610.1:c.1692-70G>T	NP_001165081.1:n.1692-70G>T
NM_007078.2:c.1677-70G>T , LRG_385t1:c.1677-70G>T	NP_009009.1:n.1677-70G>T
XM_005269464.3:c.1677-70G>T	XP_005269521.1:n.1677-70G>T
XM_005269466.3:c.1488-70G>T	XP_005269523.1:n.1488-70G>T
XM_011539184.1:c.1929-70G>T	XP_011537486.1:n.1929-70G>T
XM_011539185.1:c.1929-70G>T	XP_011537487.1:n.1929-70G>T
XM_011539186.1:c.1881-70G>T	XP_011537488.1:n.1881-70G>T
XM_011539187.1:c.1740-70G>T	XP_011537489.1:n.1740-70G>T
XM_011539188.1:c.1725-70G>T	XP_011537490.1:n.1725-70G>T
XM_011539189.1:c.1584-70G>T	XP_011537491.1:n.1584-70G>T
XM_011539190.1:c.1536-70G>T	XP_011537492.1:n.1536-70G>T
XM_011539191.1:c.1395-70G>T	XP_011537493.1:n.1395-70G>T
XM_011539192.1:c.1380-70G>T	XP_011537494.1:n.1380-70G>T
XM_011539193.1:c.885-70G>T	XP_011537495.1:n.885-70G>T
XM_011539194.1:c.696-70G>T	XP_011537496.1:n.696-70G>T
XM_005269464.4:c.1677-70G>T	XP_005269521.1:n.1677-70G>T
XM_005269466.4:c.1488-70G>T	XP_005269523.1:n.1488-70G>T
XM_011539184.2:c.1929-70G>T	XP_011537486.1:n.1929-70G>T
XM_011539185.2:c.1929-70G>T	XP_011537487.1:n.1929-70G>T
XM_011539186.2:c.1881-70G>T	XP_011537488.1:n.1881-70G>T
XM_011539187.2:c.1740-70G>T	XP_011537489.1:n.1740-70G>T
XM_011539188.2:c.1725-70G>T	XP_011537490.1:n.1725-70G>T
XM_011539190.2:c.1536-70G>T	XP_011537492.1:n.1536-70G>T
XM_011539191.2:c.1395-70G>T	XP_011537493.1:n.1395-70G>T
XM_017015606.1:c.1725-70G>T	XP_016871095.1:n.1725-70G>T
XM_017015607.1:c.885-70G>T	XP_016871096.1:n.885-70G>T
XM_024447785.1:c.1584-70G>T	XP_024303553.1:n.1584-70G>T
XM_024447786.1:c.1347-70G>T	XP_024303554.1:n.1347-70G>T
NM_001080114.2:c.1347-70G>T	NP_001073583.1:n.1347-70G>T
NM_001171610.2:c.1692-70G>T	NP_001165081.1:n.1692-70G>T
NM_001368064.1:c.1488-70G>T	NP_001354993.1:n.1488-70G>T
NM_001368065.1:c.1488-70G>T	NP_001354994.1:n.1488-70G>T
NM_001368066.1:c.1536-70G>T	NP_001354995.1:n.1536-70G>T
NM_007078.3:c.1677-70G>T MANE Select	NP_009009.1:n.1677-70G>T