Canonical Allele Identifier: CA357978075

Gene: LEF1 LEF1-AS1

Linked Data

• MyVariant Identifiers: chr4:g.109088744C>A (hg19) ; chr4:g.108167588C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108167588C>A , CM000666.2:g.108167588C>A	GRCh38
NC_000004.11:g.109088744C>A , CM000666.1:g.109088744C>A	GRCh37
NC_000004.10:g.109308193C>A	NCBI36
NG_015798.1:g.6369G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265165.6:c.180G>T (LEF1) MANE Select	ENSP00000265165.1:p.Glu60Asp
ENST00000265165.5:c.180G>T (LEF1)	ENSP00000265165.1:p.Glu60Asp
ENST00000379951.6:c.180G>T (LEF1)	ENSP00000369284.2:p.Glu60Asp
ENST00000438313.6:c.180G>T (LEF1)	ENSP00000406176.2:p.Glu60Asp
ENST00000504775.5:n.7G>T (LEF1)
ENST00000506680.5:c.180G>T (LEF1)	ENSP00000422334.1:p.Glu60Asp
NM_001130713.2:c.180G>T (LEF1)	NP_001124185.1:p.Glu60Asp
NM_001130714.2:c.180G>T (LEF1)	NP_001124186.1:p.Glu60Asp
NM_016269.4:c.180G>T (LEF1)	NP_057353.1:p.Glu60Asp
NR_029374.1:n.64C>A (LEF1-AS1)
XM_005263046.2:c.180G>T (LEF1)	XP_005263103.1:p.Glu60Asp
XM_005263046.3:c.180G>T (LEF1)	XP_005263103.1:p.Glu60Asp
NM_016269.5:c.180G>T (LEF1) MANE Select	NP_057353.1:p.Glu60Asp
NM_001130713.3:c.180G>T (LEF1)	NP_001124185.1:p.Glu60Asp
NM_001130714.3:c.180G>T (LEF1)	NP_001124186.1:p.Glu60Asp