Canonical Allele Identifier: CA815901211
Gene: LNPEP HGNC NCBI

Linked Data

dbSNP Id: rs551111525
MyVariant Identifiers: chr5:g.96320431C>A (hg19) chr5:g.96984727C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96984727C>A , CM000667.2:g.96984727C>A GRCh38
NC_000005.9:g.96320431C>A , CM000667.1:g.96320431C>A GRCh37
NC_000005.8:g.96346187C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000231368.10:c.861-353C>A MANE Select ENSP00000231368.5:n.861-353C>A
ENST00000231368.9:c.861-353C>A ENSP00000231368.5:n.861-353C>A
ENST00000395770.3:c.819-353C>A ENSP00000379117.3:n.819-353C>A
NM_005575.2:c.861-353C>A NP_005566.2:n.861-353C>A
NM_175920.3:c.819-353C>A NP_787116.2:n.819-353C>A
XM_024446045.1:c.861-353C>A XP_024301813.1:n.861-353C>A
NM_005575.3:c.861-353C>A MANE Select NP_005566.2:n.861-353C>A
NM_175920.4:c.819-353C>A NP_787116.2:n.819-353C>A
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