Canonical Allele Identifier: CA035634
Gene: LEF1 HGNC NCBI
LEF1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs267607215
MyVariant Identifiers: chr4:g.109088743A>G (hg19) chr4:g.108167587A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.108167587A>G , CM000666.2:g.108167587A>G GRCh38
NC_000004.11:g.109088743A>G , CM000666.1:g.109088743A>G GRCh37
NC_000004.10:g.109308192A>G NCBI36
NG_015798.1:g.6370T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000265165.6:c.181T>C (LEF1) MANE Select ENSP00000265165.1:p.Ser61Pro
ENST00000265165.5:c.181T>C (LEF1) ENSP00000265165.1:p.Ser61Pro
ENST00000379951.6:c.181T>C (LEF1) ENSP00000369284.2:p.Ser61Pro
ENST00000438313.6:c.181T>C (LEF1) ENSP00000406176.2:p.Ser61Pro
ENST00000504775.5:n.8T>C (LEF1)
ENST00000506680.5:c.181T>C (LEF1) ENSP00000422334.1:p.Ser61Pro
NM_001130713.2:c.181T>C (LEF1) NP_001124185.1:p.Ser61Pro
NM_001130714.2:c.181T>C (LEF1) NP_001124186.1:p.Ser61Pro
NM_016269.4:c.181T>C (LEF1) NP_057353.1:p.Ser61Pro
NR_029374.1:n.63A>G (LEF1-AS1)
XM_005263046.2:c.181T>C (LEF1) XP_005263103.1:p.Ser61Pro
XM_005263046.3:c.181T>C (LEF1) XP_005263103.1:p.Ser61Pro
NM_016269.5:c.181T>C (LEF1) MANE Select NP_057353.1:p.Ser61Pro
NM_001130713.3:c.181T>C (LEF1) NP_001124185.1:p.Ser61Pro
NM_001130714.3:c.181T>C (LEF1) NP_001124186.1:p.Ser61Pro
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