Canonical Allele Identifier: CA1742264973
Gene: LEP HGNC NCBI

Linked Data

dbSNP Id: rs1584603918

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128247155T>G , CM000669.2:g.128247155T>G GRCh38
NC_000007.13:g.127887208T>G , CM000669.1:g.127887208T>G GRCh37
NC_000007.12:g.127674444T>G NCBI36
NG_007450.1:g.10878T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000308868.5:c.-28-4836T>G MANE Select ENSP00000312652.4:n.-28-4836T>G
ENST00000308868.4:c.-28-4836T>G ENSP00000312652.4:n.-28-4836T>G
NM_000230.2:c.-28-4836T>G NP_000221.1:n.-28-4836T>G
XM_005250340.3:c.-28-4836T>G XP_005250397.1:n.-28-4836T>G
XM_005250340.5:c.-28-4836T>G XP_005250397.1:n.-28-4836T>G
NM_000230.3:c.-28-4836T>G MANE Select NP_000221.1:n.-28-4836T>G