Canonical Allele Identifier: CA1742265159
Gene: LEP HGNC NCBI

Linked Data

dbSNP Id: rs1052768273
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128247356G>T , CM000669.2:g.128247356G>T GRCh38
NC_000007.13:g.127887409G>T , CM000669.1:g.127887409G>T GRCh37
NC_000007.12:g.127674645G>T NCBI36
NG_007450.1:g.11079G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308868.5:c.-28-4635G>T MANE Select ENSP00000312652.4:n.-28-4635G>T
ENST00000308868.4:c.-28-4635G>T ENSP00000312652.4:n.-28-4635G>T
NM_000230.2:c.-28-4635G>T NP_000221.1:n.-28-4635G>T
XM_005250340.3:c.-28-4635G>T XP_005250397.1:n.-28-4635G>T
XM_005250340.5:c.-28-4635G>T XP_005250397.1:n.-28-4635G>T
NM_000230.3:c.-28-4635G>T MANE Select NP_000221.1:n.-28-4635G>T
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