Canonical Allele Identifier: CA357978095

Gene: LEF1 LEF1-AS1

Linked Data

• MyVariant Identifiers: chr4:g.109088752C>G (hg19) ; chr4:g.108167596C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108167596C>G , CM000666.2:g.108167596C>G	GRCh38
NC_000004.11:g.109088752C>G , CM000666.1:g.109088752C>G	GRCh37
NC_000004.10:g.109308201C>G	NCBI36
NG_015798.1:g.6361G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265165.6:c.172G>C (LEF1) MANE Select	ENSP00000265165.1:p.Val58Leu
ENST00000265165.5:c.172G>C (LEF1)	ENSP00000265165.1:p.Val58Leu
ENST00000379951.6:c.172G>C (LEF1)	ENSP00000369284.2:p.Val58Leu
ENST00000438313.6:c.172G>C (LEF1)	ENSP00000406176.2:p.Val58Leu
ENST00000506680.5:c.172G>C (LEF1)	ENSP00000422334.1:p.Val58Leu
NM_001130713.2:c.172G>C (LEF1)	NP_001124185.1:p.Val58Leu
NM_001130714.2:c.172G>C (LEF1)	NP_001124186.1:p.Val58Leu
NM_016269.4:c.172G>C (LEF1)	NP_057353.1:p.Val58Leu
NR_029374.1:n.72C>G (LEF1-AS1)
XM_005263046.2:c.172G>C (LEF1)	XP_005263103.1:p.Val58Leu
XM_005263046.3:c.172G>C (LEF1)	XP_005263103.1:p.Val58Leu
NM_016269.5:c.172G>C (LEF1) MANE Select	NP_057353.1:p.Val58Leu
NM_001130713.3:c.172G>C (LEF1)	NP_001124185.1:p.Val58Leu
NM_001130714.3:c.172G>C (LEF1)	NP_001124186.1:p.Val58Leu