Canonical Allele Identifier: CA785090649

Gene: LEF1

Linked Data

• dbSNP Id: rs1259668841
• gnomAD v3: 4-108125712-G-C
• gnomAD v4: 4-108125712-G-C
• MyVariant Identifiers: chr4:g.109046868G>C (hg19) ; chr4:g.108125712G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108125712G>C , CM000666.2:g.108125712G>C	GRCh38
NC_000004.11:g.109046868G>C , CM000666.1:g.109046868G>C	GRCh37
NC_000004.10:g.109266317G>C	NCBI36
NG_015798.1:g.48245C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265165.6:c.415-36455C>G MANE Select	ENSP00000265165.1:n.415-36455C>G
ENST00000265165.5:c.415-36455C>G	ENSP00000265165.1:n.415-36455C>G
ENST00000379951.6:c.415-36455C>G	ENSP00000369284.2:n.415-36455C>G
ENST00000438313.6:c.415-36455C>G	ENSP00000406176.2:n.415-36455C>G
ENST00000504775.5:n.242-36455C>G
ENST00000504950.5:c.210+37856C>G	ENSP00000427459.1:n.210+37856C>G
ENST00000505293.1:n.341-36455C>G
ENST00000506680.5:c.415-36455C>G	ENSP00000422334.1:n.415-36455C>G
ENST00000509428.5:n.234-36455C>G
ENST00000510135.5:n.294-36455C>G
ENST00000510624.5:c.211-36455C>G	ENSP00000422840.1:n.211-36455C>G
ENST00000510717.5:n.296-36455C>G
ENST00000512172.1:c.211-36455C>G	ENSP00000427365.1:n.211-36455C>G
ENST00000515500.5:c.211-36455C>G	ENSP00000422801.1:n.211-36455C>G
NM_001130713.2:c.415-36455C>G	NP_001124185.1:n.415-36455C>G
NM_001130714.2:c.415-36455C>G	NP_001124186.1:n.415-36455C>G
NM_001166119.1:c.211-36455C>G	NP_001159591.1:n.211-36455C>G
NM_016269.4:c.415-36455C>G	NP_057353.1:n.415-36455C>G
XM_005263046.2:c.415-36455C>G	XP_005263103.1:n.415-36455C>G
XM_005263047.1:c.211-36455C>G	XP_005263104.1:n.211-36455C>G
XM_005263048.1:c.211-36455C>G	XP_005263105.1:n.211-36455C>G
XM_006714233.1:c.70-36455C>G	XP_006714296.1:n.70-36455C>G
XM_005263046.3:c.415-36455C>G	XP_005263103.1:n.415-36455C>G
NM_016269.5:c.415-36455C>G MANE Select	NP_057353.1:n.415-36455C>G
NM_001130713.3:c.415-36455C>G	NP_001124185.1:n.415-36455C>G
NM_001130714.3:c.415-36455C>G	NP_001124186.1:n.415-36455C>G
NM_001166119.2:c.211-36455C>G	NP_001159591.1:n.211-36455C>G