Canonical Allele Identifier: CA1742264929
Gene: LEP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128247058T= , CM000669.2:g.128247058T= GRCh38
NC_000007.13:g.127887111T= , CM000669.1:g.127887111T= GRCh37
NC_000007.12:g.127674347T= NCBI36
NG_007450.1:g.10781T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308868.5:c.-28-4933T= MANE Select ENSP00000312652.4:n.-28-4933T=
ENST00000308868.4:c.-28-4933T= ENSP00000312652.4:n.-28-4933T=
NM_000230.2:c.-28-4933T= NP_000221.1:n.-28-4933T=
XM_005250340.3:c.-28-4933T= XP_005250397.1:n.-28-4933T=
XM_005250340.5:c.-28-4933T= XP_005250397.1:n.-28-4933T=
NM_000230.3:c.-28-4933T= MANE Select NP_000221.1:n.-28-4933T=
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