Canonical Allele Identifier: CA1742266176
Gene: LEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128248659C= , CM000669.2:g.128248659C= GRCh38
NC_000007.13:g.127888712C= , CM000669.1:g.127888712C= GRCh37
NC_000007.12:g.127675948C= NCBI36
NG_007450.1:g.12382C=

Transcript Alleles

HGVS Amino-acid change
ENST00000308868.5:c.-28-3332C= MANE Select ENSP00000312652.4:n.-28-3332C=
ENST00000308868.4:c.-28-3332C= ENSP00000312652.4:n.-28-3332C=
NM_000230.2:c.-28-3332C= NP_000221.1:n.-28-3332C=
XM_005250340.3:c.-28-3332C= XP_005250397.1:n.-28-3332C=
XM_005250340.5:c.-28-3332C= XP_005250397.1:n.-28-3332C=
NM_000230.3:c.-28-3332C= MANE Select NP_000221.1:n.-28-3332C=