Canonical Allele Identifier: CA1742266232
Gene: LEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128248722A= , CM000669.2:g.128248722A= GRCh38
NC_000007.13:g.127888775A= , CM000669.1:g.127888775A= GRCh37
NC_000007.12:g.127676011A= NCBI36
NG_007450.1:g.12445A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308868.5:c.-28-3269A= MANE Select ENSP00000312652.4:n.-28-3269A=
ENST00000308868.4:c.-28-3269A= ENSP00000312652.4:n.-28-3269A=
NM_000230.2:c.-28-3269A= NP_000221.1:n.-28-3269A=
XM_005250340.3:c.-28-3269A= XP_005250397.1:n.-28-3269A=
XM_005250340.5:c.-28-3269A= XP_005250397.1:n.-28-3269A=
NM_000230.3:c.-28-3269A= MANE Select NP_000221.1:n.-28-3269A=