Canonical Allele Identifier: CA357978079

Gene: LEF1 LEF1-AS1

Linked Data

• MyVariant Identifiers: chr4:g.109088745T>G (hg19) ; chr4:g.108167589T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108167589T>G , CM000666.2:g.108167589T>G	GRCh38
NC_000004.11:g.109088745T>G , CM000666.1:g.109088745T>G	GRCh37
NC_000004.10:g.109308194T>G	NCBI36
NG_015798.1:g.6368A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265165.6:c.179A>C (LEF1) MANE Select	ENSP00000265165.1:p.Glu60Ala
ENST00000265165.5:c.179A>C (LEF1)	ENSP00000265165.1:p.Glu60Ala
ENST00000379951.6:c.179A>C (LEF1)	ENSP00000369284.2:p.Glu60Ala
ENST00000438313.6:c.179A>C (LEF1)	ENSP00000406176.2:p.Glu60Ala
ENST00000504775.5:n.6A>C (LEF1)
ENST00000506680.5:c.179A>C (LEF1)	ENSP00000422334.1:p.Glu60Ala
NM_001130713.2:c.179A>C (LEF1)	NP_001124185.1:p.Glu60Ala
NM_001130714.2:c.179A>C (LEF1)	NP_001124186.1:p.Glu60Ala
NM_016269.4:c.179A>C (LEF1)	NP_057353.1:p.Glu60Ala
NR_029374.1:n.65T>G (LEF1-AS1)
XM_005263046.2:c.179A>C (LEF1)	XP_005263103.1:p.Glu60Ala
XM_005263046.3:c.179A>C (LEF1)	XP_005263103.1:p.Glu60Ala
NM_016269.5:c.179A>C (LEF1) MANE Select	NP_057353.1:p.Glu60Ala
NM_001130713.3:c.179A>C (LEF1)	NP_001124185.1:p.Glu60Ala
NM_001130714.3:c.179A>C (LEF1)	NP_001124186.1:p.Glu60Ala