Canonical Allele Identifier: CA1742264886
Gene: LEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128246993_128247001delinsCCACCATCT , CM000669.2:g.128246993_128247001delinsCCACCATCT GRCh38
NC_000007.13:g.127887046_127887054delinsCCACCATCT , CM000669.1:g.127887046_127887054delinsCCACCATCT GRCh37
NC_000007.12:g.127674282_127674290delinsCCACCATCT NCBI36
NG_007450.1:g.10716_10724delinsCCACCATCT

Transcript Alleles

HGVS Amino-acid change
ENST00000308868.5:c.-28-4998_-28-4990delinsCCACCATCT MANE Select ENSP00000312652.4:n.-28-4998_-28-4990deli...
ENST00000308868.4:c.-28-4998_-28-4990delinsCCACCATCT ENSP00000312652.4:n.-28-4998_-28-4990deli...
NM_000230.2:c.-28-4998_-28-4990delinsCCACCATCT NP_000221.1:n.-28-4998_-28-4990delinsCCAC...
XM_005250340.3:c.-28-4998_-28-4990delinsCCACCATCT XP_005250397.1:n.-28-4998_-28-4990delinsC...
XM_005250340.5:c.-28-4998_-28-4990delinsCCACCATCT XP_005250397.1:n.-28-4998_-28-4990delinsC...
NM_000230.3:c.-28-4998_-28-4990delinsCCACCATCT MANE Select NP_000221.1:n.-28-4998_-28-4990delinsCCAC...