Canonical Allele Identifier: CA1742266115
Gene: LEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128248577G= , CM000669.2:g.128248577G= GRCh38
NC_000007.13:g.127888630G= , CM000669.1:g.127888630G= GRCh37
NC_000007.12:g.127675866G= NCBI36
NG_007450.1:g.12300G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308868.5:c.-28-3414G= MANE Select ENSP00000312652.4:n.-28-3414G=
ENST00000308868.4:c.-28-3414G= ENSP00000312652.4:n.-28-3414G=
NM_000230.2:c.-28-3414G= NP_000221.1:n.-28-3414G=
XM_005250340.3:c.-28-3414G= XP_005250397.1:n.-28-3414G=
XM_005250340.5:c.-28-3414G= XP_005250397.1:n.-28-3414G=
NM_000230.3:c.-28-3414G= MANE Select NP_000221.1:n.-28-3414G=