Canonical Allele Identifier: CA1742265010
Gene: LEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128247181C= , CM000669.2:g.128247181C= GRCh38
NC_000007.13:g.127887234C= , CM000669.1:g.127887234C= GRCh37
NC_000007.12:g.127674470C= NCBI36
NG_007450.1:g.10904C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308868.5:c.-28-4810C= MANE Select ENSP00000312652.4:n.-28-4810C=
ENST00000308868.4:c.-28-4810C= ENSP00000312652.4:n.-28-4810C=
NM_000230.2:c.-28-4810C= NP_000221.1:n.-28-4810C=
XM_005250340.3:c.-28-4810C= XP_005250397.1:n.-28-4810C=
XM_005250340.5:c.-28-4810C= XP_005250397.1:n.-28-4810C=
NM_000230.3:c.-28-4810C= MANE Select NP_000221.1:n.-28-4810C=