Canonical Allele Identifier: CA360508127
Gene: LNPEP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.96350717T>A (hg19) chr5:g.97015013T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.97015013T>A , CM000667.2:g.97015013T>A GRCh38
NC_000005.9:g.96350717T>A , CM000667.1:g.96350717T>A GRCh37
NC_000005.8:g.96376473T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000231368.10:c.2294T>A MANE Select ENSP00000231368.5:p.Ile765Asn
ENST00000231368.9:c.2294T>A ENSP00000231368.5:p.Ile765Asn
ENST00000395770.3:c.2252T>A ENSP00000379117.3:p.Ile751Asn
NM_005575.2:c.2294T>A NP_005566.2:p.Ile765Asn
NM_175920.3:c.2252T>A NP_787116.2:p.Ile751Asn
XM_024446045.1:c.2294T>A XP_024301813.1:p.Ile765Asn
NM_005575.3:c.2294T>A MANE Select NP_005566.2:p.Ile765Asn
NM_175920.4:c.2252T>A NP_787116.2:p.Ile751Asn
Search 100 bp 5'
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