Canonical Allele Identifier: CA2564969290
Gene: LNPEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.97015012_97015013insG , CM000667.2:g.97015012_97015013insG GRCh38
NC_000005.9:g.96350716_96350717insG , CM000667.1:g.96350716_96350717insG GRCh37
NC_000005.8:g.96376472_96376473insG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000231368.10:c.2293_2294insG MANE Select ENSP00000231368.5:p.Ile765SerfsTer13
ENST00000231368.9:c.2293_2294insG ENSP00000231368.5:p.Ile765SerfsTer13
ENST00000395770.3:c.2251_2252insG ENSP00000379117.3:p.Ile751SerfsTer13
NM_005575.2:c.2293_2294insG NP_005566.2:p.Ile765SerfsTer13
NM_175920.3:c.2251_2252insG NP_787116.2:p.Ile751SerfsTer13
XM_024446045.1:c.2293_2294insG XP_024301813.1:p.Ile765SerfsTer13
NM_005575.3:c.2293_2294insG MANE Select NP_005566.2:p.Ile765SerfsTer13
NM_175920.4:c.2251_2252insG NP_787116.2:p.Ile751SerfsTer13