Canonical Allele Identifier: CA1565667881
Gene: LNPEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96984647G= , CM000667.2:g.96984647G= GRCh38
NC_000005.9:g.96320351G= , CM000667.1:g.96320351G= GRCh37
NC_000005.8:g.96346107G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000231368.10:c.861-433G= MANE Select ENSP00000231368.5:n.861-433G=
ENST00000231368.9:c.861-433G= ENSP00000231368.5:n.861-433G=
ENST00000395770.3:c.819-433G= ENSP00000379117.3:n.819-433G=
NM_005575.2:c.861-433G= NP_005566.2:n.861-433G=
NM_175920.3:c.819-433G= NP_787116.2:n.819-433G=
XM_024446045.1:c.861-433G= XP_024301813.1:n.861-433G=
NM_005575.3:c.861-433G= MANE Select NP_005566.2:n.861-433G=
NM_175920.4:c.819-433G= NP_787116.2:n.819-433G=