Canonical Allele Identifier: CA1742267166
Gene: LEP HGNC NCBI

Linked Data

dbSNP Id: rs1584605349
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128250070A>C , CM000669.2:g.128250070A>C GRCh38
NC_000007.13:g.127890123A>C , CM000669.1:g.127890123A>C GRCh37
NC_000007.12:g.127677359A>C NCBI36
NG_007450.1:g.13793A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000308868.5:c.-28-1921A>C MANE Select ENSP00000312652.4:n.-28-1921A>C
ENST00000308868.4:c.-28-1921A>C ENSP00000312652.4:n.-28-1921A>C
NM_000230.2:c.-28-1921A>C NP_000221.1:n.-28-1921A>C
XM_005250340.3:c.-28-1921A>C XP_005250397.1:n.-28-1921A>C
XM_005250340.5:c.-28-1921A>C XP_005250397.1:n.-28-1921A>C
NM_000230.3:c.-28-1921A>C MANE Select NP_000221.1:n.-28-1921A>C
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