Canonical Allele Identifier: CA103580656

Gene: LEF1

Linked Data

• dbSNP Id: rs902513060
• gnomAD v2: 4-109046884-T-TG
• gnomAD v3: 4-108125728-T-TG
• gnomAD v4: 4-108125728-T-TG
• MyVariant Identifiers: chr4:g.109046884_109046885insG (hg19) ; chr4:g.108125728_108125729insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108125728_108125729insG , CM000666.2:g.108125728_108125729insG	GRCh38
NC_000004.11:g.109046884_109046885insG , CM000666.1:g.109046884_109046885insG	GRCh37
NC_000004.10:g.109266333_109266334insG	NCBI36
NG_015798.1:g.48228_48229insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265165.6:c.415-36472_415-36471insC MANE Select	ENSP00000265165.1:n.415-36472_415-36471insC
ENST00000265165.5:c.415-36472_415-36471insC	ENSP00000265165.1:n.415-36472_415-36471insC
ENST00000379951.6:c.415-36472_415-36471insC	ENSP00000369284.2:n.415-36472_415-36471insC
ENST00000438313.6:c.415-36472_415-36471insC	ENSP00000406176.2:n.415-36472_415-36471insC
ENST00000504775.5:n.242-36472_242-36471insC
ENST00000504950.5:c.210+37839_210+37840insC	ENSP00000427459.1:n.210+37839_210+37840insC
ENST00000505293.1:n.341-36472_341-36471insC
ENST00000506680.5:c.415-36472_415-36471insC	ENSP00000422334.1:n.415-36472_415-36471insC
ENST00000509428.5:n.234-36472_234-36471insC
ENST00000510135.5:n.294-36472_294-36471insC
ENST00000510624.5:c.211-36472_211-36471insC	ENSP00000422840.1:n.211-36472_211-36471insC
ENST00000510717.5:n.296-36472_296-36471insC
ENST00000512172.1:c.211-36472_211-36471insC	ENSP00000427365.1:n.211-36472_211-36471insC
ENST00000515500.5:c.211-36472_211-36471insC	ENSP00000422801.1:n.211-36472_211-36471insC
NM_001130713.2:c.415-36472_415-36471insC	NP_001124185.1:n.415-36472_415-36471insC
NM_001130714.2:c.415-36472_415-36471insC	NP_001124186.1:n.415-36472_415-36471insC
NM_001166119.1:c.211-36472_211-36471insC	NP_001159591.1:n.211-36472_211-36471insC
NM_016269.4:c.415-36472_415-36471insC	NP_057353.1:n.415-36472_415-36471insC
XM_005263046.2:c.415-36472_415-36471insC	XP_005263103.1:n.415-36472_415-36471insC
XM_005263047.1:c.211-36472_211-36471insC	XP_005263104.1:n.211-36472_211-36471insC
XM_005263048.1:c.211-36472_211-36471insC	XP_005263105.1:n.211-36472_211-36471insC
XM_006714233.1:c.70-36472_70-36471insC	XP_006714296.1:n.70-36472_70-36471insC
XM_005263046.3:c.415-36472_415-36471insC	XP_005263103.1:n.415-36472_415-36471insC
NM_016269.5:c.415-36472_415-36471insC MANE Select	NP_057353.1:n.415-36472_415-36471insC
NM_001130713.3:c.415-36472_415-36471insC	NP_001124185.1:n.415-36472_415-36471insC
NM_001130714.3:c.415-36472_415-36471insC	NP_001124186.1:n.415-36472_415-36471insC
NM_001166119.2:c.211-36472_211-36471insC	NP_001159591.1:n.211-36472_211-36471insC