Canonical Allele Identifier: CA2580616750
Gene: LEF1 HGNC NCBI
LEF1-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.108167700_108167702dup , CM000666.2:g.108167700_108167702dup GRCh38
NC_000004.11:g.109088856_109088858dup , CM000666.1:g.109088856_109088858dup GRCh37
NC_000004.10:g.109308305_109308307dup NCBI36
NG_015798.1:g.6258_6260dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000265165.6:c.69_71dup (LEF1) MANE Select ENSP00000265165.1:p.Met23_Ile24insMet
ENST00000265165.5:c.69_71dup (LEF1) ENSP00000265165.1:p.Met23_Ile24insMet
ENST00000379951.6:c.69_71dup (LEF1) ENSP00000369284.2:p.Met23_Ile24insMet
ENST00000438313.6:c.69_71dup (LEF1) ENSP00000406176.2:p.Met23_Ile24insMet
ENST00000506680.5:c.69_71dup (LEF1) ENSP00000422334.1:p.Met23_Ile24insMet
NM_001130713.2:c.69_71dup (LEF1) NP_001124185.1:p.Met23_Ile24insMet
NM_001130714.2:c.69_71dup (LEF1) NP_001124186.1:p.Met23_Ile24insMet
NM_016269.4:c.69_71dup (LEF1) NP_057353.1:p.Met23_Ile24insMet
NR_029374.1:n.176_178dup (LEF1-AS1)
XM_005263046.2:c.69_71dup (LEF1) XP_005263103.1:p.Met23_Ile24insMet
XM_005263046.3:c.69_71dup (LEF1) XP_005263103.1:p.Met23_Ile24insMet
NM_016269.5:c.69_71dup (LEF1) MANE Select NP_057353.1:p.Met23_Ile24insMet
NM_001130713.3:c.69_71dup (LEF1) NP_001124185.1:p.Met23_Ile24insMet
NM_001130714.3:c.69_71dup (LEF1) NP_001124186.1:p.Met23_Ile24insMet
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