Canonical Allele Identifier: CA1742267163
Gene: LEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128250069_128250070delinsGA , CM000669.2:g.128250069_128250070delinsGA GRCh38
NC_000007.13:g.127890122_127890123delinsGA , CM000669.1:g.127890122_127890123delinsGA GRCh37
NC_000007.12:g.127677358_127677359delinsGA NCBI36
NG_007450.1:g.13792_13793delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000308868.5:c.-28-1922_-28-1921delinsGA MANE Select ENSP00000312652.4:n.-28-1922_-28-1921deli...
ENST00000308868.4:c.-28-1922_-28-1921delinsGA ENSP00000312652.4:n.-28-1922_-28-1921deli...
NM_000230.2:c.-28-1922_-28-1921delinsGA NP_000221.1:n.-28-1922_-28-1921delinsGA
XM_005250340.3:c.-28-1922_-28-1921delinsGA XP_005250397.1:n.-28-1922_-28-1921delinsG...
XM_005250340.5:c.-28-1922_-28-1921delinsGA XP_005250397.1:n.-28-1922_-28-1921delinsG...
NM_000230.3:c.-28-1922_-28-1921delinsGA MANE Select NP_000221.1:n.-28-1922_-28-1921delinsGA