Canonical Allele Identifier: CA1483995999
Gene: LEF1 HGNC NCBI

Linked Data

dbSNP Id: rs956237

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.108125804G>C , CM000666.2:g.108125804G>C GRCh38
NC_000004.11:g.109046960G>C , CM000666.1:g.109046960G>C GRCh37
NC_000004.10:g.109266409G>C NCBI36
NG_015798.1:g.48153C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000265165.6:c.415-36547C>G MANE Select ENSP00000265165.1:n.415-36547C>G
ENST00000265165.5:c.415-36547C>G ENSP00000265165.1:n.415-36547C>G
ENST00000379951.6:c.415-36547C>G ENSP00000369284.2:n.415-36547C>G
ENST00000438313.6:c.415-36547C>G ENSP00000406176.2:n.415-36547C>G
ENST00000504775.5:n.242-36547C>G
ENST00000504950.5:c.210+37764C>G ENSP00000427459.1:n.210+37764C>G
ENST00000505293.1:n.341-36547C>G
ENST00000506680.5:c.415-36547C>G ENSP00000422334.1:n.415-36547C>G
ENST00000509428.5:n.234-36547C>G
ENST00000510135.5:n.294-36547C>G
ENST00000510624.5:c.211-36547C>G ENSP00000422840.1:n.211-36547C>G
ENST00000510717.5:n.296-36547C>G
ENST00000512172.1:c.211-36547C>G ENSP00000427365.1:n.211-36547C>G
ENST00000515500.5:c.211-36547C>G ENSP00000422801.1:n.211-36547C>G
NM_001130713.2:c.415-36547C>G NP_001124185.1:n.415-36547C>G
NM_001130714.2:c.415-36547C>G NP_001124186.1:n.415-36547C>G
NM_001166119.1:c.211-36547C>G NP_001159591.1:n.211-36547C>G
NM_016269.4:c.415-36547C>G NP_057353.1:n.415-36547C>G
XM_005263046.2:c.415-36547C>G XP_005263103.1:n.415-36547C>G
XM_005263047.1:c.211-36547C>G XP_005263104.1:n.211-36547C>G
XM_005263048.1:c.211-36547C>G XP_005263105.1:n.211-36547C>G
XM_006714233.1:c.70-36547C>G XP_006714296.1:n.70-36547C>G
XM_005263046.3:c.415-36547C>G XP_005263103.1:n.415-36547C>G
NM_016269.5:c.415-36547C>G MANE Select NP_057353.1:n.415-36547C>G
NM_001130713.3:c.415-36547C>G NP_001124185.1:n.415-36547C>G
NM_001130714.3:c.415-36547C>G NP_001124186.1:n.415-36547C>G
NM_001166119.2:c.211-36547C>G NP_001159591.1:n.211-36547C>G