Canonical Allele Identifier: CA360508160
Gene: LNPEP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.96350723A>C (hg19) chr5:g.97015019A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.97015019A>C , CM000667.2:g.97015019A>C GRCh38
NC_000005.9:g.96350723A>C , CM000667.1:g.96350723A>C GRCh37
NC_000005.8:g.96376479A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000231368.10:c.2300A>C MANE Select ENSP00000231368.5:p.Glu767Ala
ENST00000231368.9:c.2300A>C ENSP00000231368.5:p.Glu767Ala
ENST00000395770.3:c.2258A>C ENSP00000379117.3:p.Glu753Ala
NM_005575.2:c.2300A>C NP_005566.2:p.Glu767Ala
NM_175920.3:c.2258A>C NP_787116.2:p.Glu753Ala
XM_024446045.1:c.2300A>C XP_024301813.1:p.Glu767Ala
NM_005575.3:c.2300A>C MANE Select NP_005566.2:p.Glu767Ala
NM_175920.4:c.2258A>C NP_787116.2:p.Glu753Ala
Search 100 bp 5'
Search 100 bp 3'