Canonical Allele Identifier: CA166743535

Gene: LEP

Linked Data

• dbSNP Id: rs964381856
• MyVariant Identifiers: chr7:g.127887255A>C (hg19) ; chr7:g.128247202A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128247202A>C , CM000669.2:g.128247202A>C	GRCh38
NC_000007.13:g.127887255A>C , CM000669.1:g.127887255A>C	GRCh37
NC_000007.12:g.127674491A>C	NCBI36
NG_007450.1:g.10925A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308868.5:c.-28-4789A>C MANE Select	ENSP00000312652.4:n.-28-4789A>C
ENST00000308868.4:c.-28-4789A>C	ENSP00000312652.4:n.-28-4789A>C
NM_000230.2:c.-28-4789A>C	NP_000221.1:n.-28-4789A>C
XM_005250340.3:c.-28-4789A>C	XP_005250397.1:n.-28-4789A>C
XM_005250340.5:c.-28-4789A>C	XP_005250397.1:n.-28-4789A>C
NM_000230.3:c.-28-4789A>C MANE Select	NP_000221.1:n.-28-4789A>C