Canonical Allele Identifier: CA1742267142
Gene: LEP HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128250050C= , CM000669.2:g.128250050C= GRCh38
NC_000007.13:g.127890103C= , CM000669.1:g.127890103C= GRCh37
NC_000007.12:g.127677339C= NCBI36
NG_007450.1:g.13773C=

Transcript Alleles

HGVS Amino-acid change
ENST00000308868.5:c.-28-1941C= MANE Select ENSP00000312652.4:n.-28-1941C=
ENST00000308868.4:c.-28-1941C= ENSP00000312652.4:n.-28-1941C=
NM_000230.2:c.-28-1941C= NP_000221.1:n.-28-1941C=
XM_005250340.3:c.-28-1941C= XP_005250397.1:n.-28-1941C=
XM_005250340.5:c.-28-1941C= XP_005250397.1:n.-28-1941C=
NM_000230.3:c.-28-1941C= MANE Select NP_000221.1:n.-28-1941C=
Search 100 bp 5'
Search 100 bp 3'