Canonical Allele Identifier: CA457857399
Gene: LEP HGNC NCBI

Linked Data

gnomAD v4: 7-128254580-T-A
MyVariant Identifiers: chr7:g.127894633T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128254580T>A , CM000669.2:g.128254580T>A GRCh38
NC_000007.13:g.127894633T>A , CM000669.1:g.127894633T>A GRCh37
NC_000007.12:g.127681869T>A NCBI36
NG_007450.1:g.18303T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000308868.5:c.321T>A MANE Select ENSP00000312652.4:p.Leu107=
ENST00000308868.4:c.321T>A ENSP00000312652.4:p.Leu107=
NM_000230.2:c.321T>A NP_000221.1:p.Leu107=
XM_005250340.3:c.318T>A XP_005250397.1:p.Leu106=
XM_005250340.5:c.318T>A XP_005250397.1:p.Leu106=
NM_000230.3:c.321T>A MANE Select NP_000221.1:p.Leu107=
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