Canonical Allele Identifier: CA10623195
Gene: LEP HGNC NCBI

Linked Data

ClinVar Variation Id: 358828
dbSNP Id: rs886061975

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128255185G>C , CM000669.2:g.128255185G>C GRCh38
NC_000007.13:g.127895238G>C , CM000669.1:g.127895238G>C GRCh37
NC_000007.12:g.127682474G>C NCBI36
NG_007450.1:g.18908G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308868.5:c.*422G>C MANE Select ENSP00000312652.4:n.*422G>C
ENST00000308868.4:c.*422G>C ENSP00000312652.4:n.*422G>C
NM_000230.2:c.*422G>C NP_000221.1:n.*422G>C
XM_005250340.3:c.*422G>C XP_005250397.1:n.*422G>C
XM_005250340.5:c.*422G>C XP_005250397.1:n.*422G>C
NM_000230.3:c.*422G>C MANE Select NP_000221.1:n.*422G>C