Canonical Allele Identifier: CA357978102

Gene: LEF1 LEF1-AS1

Linked Data

• MyVariant Identifiers: chr4:g.109088755A>C (hg19) ; chr4:g.108167599A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108167599A>C , CM000666.2:g.108167599A>C	GRCh38
NC_000004.11:g.109088755A>C , CM000666.1:g.109088755A>C	GRCh37
NC_000004.10:g.109308204A>C	NCBI36
NG_015798.1:g.6358T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265165.6:c.169T>G (LEF1) MANE Select	ENSP00000265165.1:p.Leu57Val
ENST00000265165.5:c.169T>G (LEF1)	ENSP00000265165.1:p.Leu57Val
ENST00000379951.6:c.169T>G (LEF1)	ENSP00000369284.2:p.Leu57Val
ENST00000438313.6:c.169T>G (LEF1)	ENSP00000406176.2:p.Leu57Val
ENST00000506680.5:c.169T>G (LEF1)	ENSP00000422334.1:p.Leu57Val
NM_001130713.2:c.169T>G (LEF1)	NP_001124185.1:p.Leu57Val
NM_001130714.2:c.169T>G (LEF1)	NP_001124186.1:p.Leu57Val
NM_016269.4:c.169T>G (LEF1)	NP_057353.1:p.Leu57Val
NR_029374.1:n.75A>C (LEF1-AS1)
XM_005263046.2:c.169T>G (LEF1)	XP_005263103.1:p.Leu57Val
XM_005263046.3:c.169T>G (LEF1)	XP_005263103.1:p.Leu57Val
NM_016269.5:c.169T>G (LEF1) MANE Select	NP_057353.1:p.Leu57Val
NM_001130713.3:c.169T>G (LEF1)	NP_001124185.1:p.Leu57Val
NM_001130714.3:c.169T>G (LEF1)	NP_001124186.1:p.Leu57Val