Canonical Allele Identifier: CA1565681212
Gene: LNPEP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.97014909A= , CM000667.2:g.97014909A= GRCh38
NC_000005.9:g.96350613A= , CM000667.1:g.96350613A= GRCh37
NC_000005.8:g.96376369A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000231368.10:c.2220-30A= MANE Select ENSP00000231368.5:n.2220-30A=
ENST00000231368.9:c.2220-30A= ENSP00000231368.5:n.2220-30A=
ENST00000395770.3:c.2178-30A= ENSP00000379117.3:n.2178-30A=
NM_005575.2:c.2220-30A= NP_005566.2:n.2220-30A=
NM_175920.3:c.2178-30A= NP_787116.2:n.2178-30A=
XM_024446045.1:c.2220-30A= XP_024301813.1:n.2220-30A=
NM_005575.3:c.2220-30A= MANE Select NP_005566.2:n.2220-30A=
NM_175920.4:c.2178-30A= NP_787116.2:n.2178-30A=
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