Canonical Allele Identifier: CA360508521

Gene: LNPEP

Linked Data

• dbSNP Id: rs1791032410
• gnomAD v3: 5-97015078-C-G
• gnomAD v4: 5-97015078-C-G
• MyVariant Identifiers: chr5:g.96350782C>G (hg19) ; chr5:g.97015078C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.97015078C>G , CM000667.2:g.97015078C>G	GRCh38
NC_000005.9:g.96350782C>G , CM000667.1:g.96350782C>G	GRCh37
NC_000005.8:g.96376538C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231368.10:c.2359C>G MANE Select	ENSP00000231368.5:p.Leu787Val
ENST00000231368.9:c.2359C>G	ENSP00000231368.5:p.Leu787Val
ENST00000395770.3:c.2317C>G	ENSP00000379117.3:p.Leu773Val
NM_005575.2:c.2359C>G	NP_005566.2:p.Leu787Val
NM_175920.3:c.2317C>G	NP_787116.2:p.Leu773Val
XM_024446045.1:c.2359C>G	XP_024301813.1:p.Leu787Val
NM_005575.3:c.2359C>G MANE Select	NP_005566.2:p.Leu787Val
NM_175920.4:c.2317C>G	NP_787116.2:p.Leu773Val