Canonical Allele Identifier: CA1565667955
Gene: LNPEP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96984802G= , CM000667.2:g.96984802G= GRCh38
NC_000005.9:g.96320506G= , CM000667.1:g.96320506G= GRCh37
NC_000005.8:g.96346262G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000231368.10:c.861-278G= MANE Select ENSP00000231368.5:n.861-278G=
ENST00000231368.9:c.861-278G= ENSP00000231368.5:n.861-278G=
ENST00000395770.3:c.819-278G= ENSP00000379117.3:n.819-278G=
NM_005575.2:c.861-278G= NP_005566.2:n.861-278G=
NM_175920.3:c.819-278G= NP_787116.2:n.819-278G=
XM_024446045.1:c.861-278G= XP_024301813.1:n.861-278G=
NM_005575.3:c.861-278G= MANE Select NP_005566.2:n.861-278G=
NM_175920.4:c.819-278G= NP_787116.2:n.819-278G=
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