Canonical Allele Identifier: CA2609994709

Gene: LDB3

Linked Data

• gnomAD v4: 10-86668422-G-GTAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86668422_86668423insTAT , CM000672.2:g.86668422_86668423insTAT	GRCh38
NC_000010.10:g.88428179_88428180insTAT , CM000672.1:g.88428179_88428180insTAT	GRCh37
NC_000010.9:g.88418159_88418160insTAT	NCBI36
NG_008876.1:g.4859_4860insTAT , LRG_385:g.4859_4860insTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443292.2:c.1487-247_1487-246insTAT	ENSP00000393132.2:n.1487-247_1487-246insTAT
ENST00000685347.1:n.1449-247_1449-246insTAT
ENST00000687856.1:c.-23-247_-23-246insTAT	ENSP00000510221.1:n.-23-247_-23-246insTAT
ENST00000688001.1:c.-23-247_-23-246insTAT	ENSP00000508987.1:n.-23-247_-23-246insTAT
ENST00000688785.1:c.-23-247_-23-246insTAT	ENSP00000509572.1:n.-23-247_-23-246insTAT
ENST00000691462.1:c.-23-247_-23-246insTAT	ENSP00000509930.1:n.-23-247_-23-246insTAT
ENST00000692941.1:n.2070-247_2070-246insTAT
XM_005269464.3:c.-172_-171insTAT	XP_005269521.1:n.-172_-171insTAT
XM_005269466.3:c.-172_-171insTAT	XP_005269523.1:n.-172_-171insTAT
XM_005269468.3:c.-172_-171insTAT	XP_005269525.1:n.-172_-171insTAT
XM_011539184.1:c.-172_-171insTAT	XP_011537486.1:n.-172_-171insTAT
XM_011539185.1:c.-23-247_-23-246insTAT	XP_011537487.1:n.-23-247_-23-246insTAT
XM_011539186.1:c.-172_-171insTAT	XP_011537488.1:n.-172_-171insTAT
XM_011539187.1:c.-172_-171insTAT	XP_011537489.1:n.-172_-171insTAT
XM_011539188.1:c.-172_-171insTAT	XP_011537490.1:n.-172_-171insTAT
XM_011539189.1:c.-23-247_-23-246insTAT	XP_011537491.1:n.-23-247_-23-246insTAT
XM_011539191.1:c.-172_-171insTAT	XP_011537493.1:n.-172_-171insTAT
XM_011539192.1:c.-172_-171insTAT	XP_011537494.1:n.-172_-171insTAT
XM_011539193.1:c.-495-247_-495-246insTAT	XP_011537495.1:n.-495-247_-495-246insTAT
XM_011539194.1:c.-495-247_-495-246insTAT	XP_011537496.1:n.-495-247_-495-246insTAT
XM_011539195.1:c.-172_-171insTAT	XP_011537497.1:n.-172_-171insTAT
XM_005269464.4:c.-172_-171insTAT	XP_005269521.1:n.-172_-171insTAT
XM_005269466.4:c.-172_-171insTAT	XP_005269523.1:n.-172_-171insTAT
XM_005269468.4:c.-172_-171insTAT	XP_005269525.1:n.-172_-171insTAT
XM_011539184.2:c.-172_-171insTAT	XP_011537486.1:n.-172_-171insTAT
XM_011539185.2:c.-23-247_-23-246insTAT	XP_011537487.1:n.-23-247_-23-246insTAT
XM_011539186.2:c.-172_-171insTAT	XP_011537488.1:n.-172_-171insTAT
XM_011539187.2:c.-172_-171insTAT	XP_011537489.1:n.-172_-171insTAT
XM_011539188.2:c.-172_-171insTAT	XP_011537490.1:n.-172_-171insTAT
XM_011539190.2:c.-172_-171insTAT	XP_011537492.1:n.-172_-171insTAT
XM_011539191.2:c.-172_-171insTAT	XP_011537493.1:n.-172_-171insTAT
XM_011539195.2:c.-172_-171insTAT	XP_011537497.1:n.-172_-171insTAT
XM_017015606.1:c.-23-247_-23-246insTAT	XP_016871095.1:n.-23-247_-23-246insTAT
XM_017015608.1:c.-23-247_-23-246insTAT	XP_016871097.1:n.-23-247_-23-246insTAT
XM_017015609.1:c.-23-247_-23-246insTAT	XP_016871098.1:n.-23-247_-23-246insTAT
XM_024447785.1:c.-172_-171insTAT	XP_024303553.1:n.-172_-171insTAT
XM_024447786.1:c.-172_-171insTAT	XP_024303554.1:n.-172_-171insTAT
XM_024447787.1:c.-172_-171insTAT	XP_024303555.1:n.-172_-171insTAT
NM_001368063.1:c.-23-247_-23-246insTAT	NP_001354992.1:n.-23-247_-23-246insTAT
NM_001368064.1:c.-23-247_-23-246insTAT	NP_001354993.1:n.-23-247_-23-246insTAT
NM_001368068.1:c.-23-247_-23-246insTAT	NP_001354997.1:n.-23-247_-23-246insTAT