Canonical Allele Identifier: CA357978091

Gene: LEF1 LEF1-AS1

Linked Data

• MyVariant Identifiers: chr4:g.109088751A>C (hg19) ; chr4:g.108167595A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108167595A>C , CM000666.2:g.108167595A>C	GRCh38
NC_000004.11:g.109088751A>C , CM000666.1:g.109088751A>C	GRCh37
NC_000004.10:g.109308200A>C	NCBI36
NG_015798.1:g.6362T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265165.6:c.173T>G (LEF1) MANE Select	ENSP00000265165.1:p.Val58Gly
ENST00000265165.5:c.173T>G (LEF1)	ENSP00000265165.1:p.Val58Gly
ENST00000379951.6:c.173T>G (LEF1)	ENSP00000369284.2:p.Val58Gly
ENST00000438313.6:c.173T>G (LEF1)	ENSP00000406176.2:p.Val58Gly
ENST00000506680.5:c.173T>G (LEF1)	ENSP00000422334.1:p.Val58Gly
NM_001130713.2:c.173T>G (LEF1)	NP_001124185.1:p.Val58Gly
NM_001130714.2:c.173T>G (LEF1)	NP_001124186.1:p.Val58Gly
NM_016269.4:c.173T>G (LEF1)	NP_057353.1:p.Val58Gly
NR_029374.1:n.71A>C (LEF1-AS1)
XM_005263046.2:c.173T>G (LEF1)	XP_005263103.1:p.Val58Gly
XM_005263046.3:c.173T>G (LEF1)	XP_005263103.1:p.Val58Gly
NM_016269.5:c.173T>G (LEF1) MANE Select	NP_057353.1:p.Val58Gly
NM_001130713.3:c.173T>G (LEF1)	NP_001124185.1:p.Val58Gly
NM_001130714.3:c.173T>G (LEF1)	NP_001124186.1:p.Val58Gly