Canonical Allele Identifier: CA360508194
Gene: LNPEP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.96350731T>C (hg19) chr5:g.97015027T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.97015027T>C , CM000667.2:g.97015027T>C GRCh38
NC_000005.9:g.96350731T>C , CM000667.1:g.96350731T>C GRCh37
NC_000005.8:g.96376487T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000231368.10:c.2308T>C MANE Select ENSP00000231368.5:p.Phe770Leu
ENST00000231368.9:c.2308T>C ENSP00000231368.5:p.Phe770Leu
ENST00000395770.3:c.2266T>C ENSP00000379117.3:p.Phe756Leu
NM_005575.2:c.2308T>C NP_005566.2:p.Phe770Leu
NM_175920.3:c.2266T>C NP_787116.2:p.Phe756Leu
XM_024446045.1:c.2308T>C XP_024301813.1:p.Phe770Leu
NM_005575.3:c.2308T>C MANE Select NP_005566.2:p.Phe770Leu
NM_175920.4:c.2266T>C NP_787116.2:p.Phe756Leu
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