Canonical Allele Identifier: CA1742264939
Gene: LEP HGNC NCBI

Linked Data

dbSNP Id: rs1795219784
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128247081del , CM000669.2:g.128247081del GRCh38
NC_000007.13:g.127887134del , CM000669.1:g.127887134del GRCh37
NC_000007.12:g.127674370del NCBI36
NG_007450.1:g.10804del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308868.5:c.-28-4910del MANE Select ENSP00000312652.4:n.-28-4910del
ENST00000308868.4:c.-28-4910del ENSP00000312652.4:n.-28-4910del
NM_000230.2:c.-28-4910del NP_000221.1:n.-28-4910del
XM_005250340.3:c.-28-4910del XP_005250397.1:n.-28-4910del
XM_005250340.5:c.-28-4910del XP_005250397.1:n.-28-4910del
NM_000230.3:c.-28-4910del MANE Select NP_000221.1:n.-28-4910del
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