Canonical Allele Identifier: CA103580655

Gene: LEF1

Linked Data

• dbSNP Id: rs1553956704
• MyVariant Identifiers: chr4:g.109046880_109046881insTG (hg19) ; chr4:g.108125724_108125725insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108125725_108125726insGT , CM000666.2:g.108125725_108125726insGT	GRCh38
NC_000004.11:g.109046881_109046882insGT , CM000666.1:g.109046881_109046882insGT	GRCh37
NC_000004.10:g.109266330_109266331insGT	NCBI36
NG_015798.1:g.48232_48233insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265165.6:c.415-36468_415-36467insCA MANE Select	ENSP00000265165.1:n.415-36468_415-36467insCA
ENST00000265165.5:c.415-36468_415-36467insCA	ENSP00000265165.1:n.415-36468_415-36467insCA
ENST00000379951.6:c.415-36468_415-36467insCA	ENSP00000369284.2:n.415-36468_415-36467insCA
ENST00000438313.6:c.415-36468_415-36467insCA	ENSP00000406176.2:n.415-36468_415-36467insCA
ENST00000504775.5:n.242-36468_242-36467insCA
ENST00000504950.5:c.210+37843_210+37844insCA	ENSP00000427459.1:n.210+37843_210+37844insCA
ENST00000505293.1:n.341-36468_341-36467insCA
ENST00000506680.5:c.415-36468_415-36467insCA	ENSP00000422334.1:n.415-36468_415-36467insCA
ENST00000509428.5:n.234-36468_234-36467insCA
ENST00000510135.5:n.294-36468_294-36467insCA
ENST00000510624.5:c.211-36468_211-36467insCA	ENSP00000422840.1:n.211-36468_211-36467insCA
ENST00000510717.5:n.296-36468_296-36467insCA
ENST00000512172.1:c.211-36468_211-36467insCA	ENSP00000427365.1:n.211-36468_211-36467insCA
ENST00000515500.5:c.211-36468_211-36467insCA	ENSP00000422801.1:n.211-36468_211-36467insCA
NM_001130713.2:c.415-36468_415-36467insCA	NP_001124185.1:n.415-36468_415-36467insCA
NM_001130714.2:c.415-36468_415-36467insCA	NP_001124186.1:n.415-36468_415-36467insCA
NM_001166119.1:c.211-36468_211-36467insCA	NP_001159591.1:n.211-36468_211-36467insCA
NM_016269.4:c.415-36468_415-36467insCA	NP_057353.1:n.415-36468_415-36467insCA
XM_005263046.2:c.415-36468_415-36467insCA	XP_005263103.1:n.415-36468_415-36467insCA
XM_005263047.1:c.211-36468_211-36467insCA	XP_005263104.1:n.211-36468_211-36467insCA
XM_005263048.1:c.211-36468_211-36467insCA	XP_005263105.1:n.211-36468_211-36467insCA
XM_006714233.1:c.70-36468_70-36467insCA	XP_006714296.1:n.70-36468_70-36467insCA
XM_005263046.3:c.415-36468_415-36467insCA	XP_005263103.1:n.415-36468_415-36467insCA
NM_016269.5:c.415-36468_415-36467insCA MANE Select	NP_057353.1:n.415-36468_415-36467insCA
NM_001130713.3:c.415-36468_415-36467insCA	NP_001124185.1:n.415-36468_415-36467insCA
NM_001130714.3:c.415-36468_415-36467insCA	NP_001124186.1:n.415-36468_415-36467insCA
NM_001166119.2:c.211-36468_211-36467insCA	NP_001159591.1:n.211-36468_211-36467insCA