Canonical Allele Identifier: CA1483995970

Gene: LEF1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108125729_108125737delinsTAGCACGCA , CM000666.2:g.108125729_108125737delinsTAGCACGCA	GRCh38
NC_000004.11:g.109046885_109046893delinsTAGCACGCA , CM000666.1:g.109046885_109046893delinsTAGCACGCA	GRCh37
NC_000004.10:g.109266334_109266342delinsTAGCACGCA	NCBI36
NG_015798.1:g.48220_48228delinsTGCGTGCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265165.6:c.415-36480_415-36472delinsTGCGTGCTA MANE Select	ENSP00000265165.1:n.415-36480_415-36472delinsTGCGTGCTA
ENST00000265165.5:c.415-36480_415-36472delinsTGCGTGCTA	ENSP00000265165.1:n.415-36480_415-36472delinsTGCGTGCTA
ENST00000379951.6:c.415-36480_415-36472delinsTGCGTGCTA	ENSP00000369284.2:n.415-36480_415-36472delinsTGCGTGCTA
ENST00000438313.6:c.415-36480_415-36472delinsTGCGTGCTA	ENSP00000406176.2:n.415-36480_415-36472delinsTGCGTGCTA
ENST00000504775.5:n.242-36480_242-36472delinsTGCGTGCTA
ENST00000504950.5:c.210+37831_210+37839delinsTGCGTGCTA	ENSP00000427459.1:n.210+37831_210+37839delinsTGCGTGCTA
ENST00000505293.1:n.341-36480_341-36472delinsTGCGTGCTA
ENST00000506680.5:c.415-36480_415-36472delinsTGCGTGCTA	ENSP00000422334.1:n.415-36480_415-36472delinsTGCGTGCTA
ENST00000509428.5:n.234-36480_234-36472delinsTGCGTGCTA
ENST00000510135.5:n.294-36480_294-36472delinsTGCGTGCTA
ENST00000510624.5:c.211-36480_211-36472delinsTGCGTGCTA	ENSP00000422840.1:n.211-36480_211-36472delinsTGCGTGCTA
ENST00000510717.5:n.296-36480_296-36472delinsTGCGTGCTA
ENST00000512172.1:c.211-36480_211-36472delinsTGCGTGCTA	ENSP00000427365.1:n.211-36480_211-36472delinsTGCGTGCTA
ENST00000515500.5:c.211-36480_211-36472delinsTGCGTGCTA	ENSP00000422801.1:n.211-36480_211-36472delinsTGCGTGCTA
NM_001130713.2:c.415-36480_415-36472delinsTGCGTGCTA	NP_001124185.1:n.415-36480_415-36472delinsTGCGTGCTA
NM_001130714.2:c.415-36480_415-36472delinsTGCGTGCTA	NP_001124186.1:n.415-36480_415-36472delinsTGCGTGCTA
NM_001166119.1:c.211-36480_211-36472delinsTGCGTGCTA	NP_001159591.1:n.211-36480_211-36472delinsTGCGTGCTA
NM_016269.4:c.415-36480_415-36472delinsTGCGTGCTA	NP_057353.1:n.415-36480_415-36472delinsTGCGTGCTA
XM_005263046.2:c.415-36480_415-36472delinsTGCGTGCTA	XP_005263103.1:n.415-36480_415-36472delinsTGCGTGCTA
XM_005263047.1:c.211-36480_211-36472delinsTGCGTGCTA	XP_005263104.1:n.211-36480_211-36472delinsTGCGTGCTA
XM_005263048.1:c.211-36480_211-36472delinsTGCGTGCTA	XP_005263105.1:n.211-36480_211-36472delinsTGCGTGCTA
XM_006714233.1:c.70-36480_70-36472delinsTGCGTGCTA	XP_006714296.1:n.70-36480_70-36472delinsTGCGTGCTA
XM_005263046.3:c.415-36480_415-36472delinsTGCGTGCTA	XP_005263103.1:n.415-36480_415-36472delinsTGCGTGCTA
NM_016269.5:c.415-36480_415-36472delinsTGCGTGCTA MANE Select	NP_057353.1:n.415-36480_415-36472delinsTGCGTGCTA
NM_001130713.3:c.415-36480_415-36472delinsTGCGTGCTA	NP_001124185.1:n.415-36480_415-36472delinsTGCGTGCTA
NM_001130714.3:c.415-36480_415-36472delinsTGCGTGCTA	NP_001124186.1:n.415-36480_415-36472delinsTGCGTGCTA
NM_001166119.2:c.211-36480_211-36472delinsTGCGTGCTA	NP_001159591.1:n.211-36480_211-36472delinsTGCGTGCTA