Canonical Allele Identifier: CA1565667890
Gene: LNPEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96984665_96984667delinsAAC , CM000667.2:g.96984665_96984667delinsAAC GRCh38
NC_000005.9:g.96320369_96320371delinsAAC , CM000667.1:g.96320369_96320371delinsAAC GRCh37
NC_000005.8:g.96346125_96346127delinsAAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000231368.10:c.861-415_861-413delinsAAC MANE Select ENSP00000231368.5:n.861-415_861-413delinsAAC
ENST00000231368.9:c.861-415_861-413delinsAAC ENSP00000231368.5:n.861-415_861-413delinsAAC
ENST00000395770.3:c.819-415_819-413delinsAAC ENSP00000379117.3:n.819-415_819-413delinsAAC
NM_005575.2:c.861-415_861-413delinsAAC NP_005566.2:n.861-415_861-413delinsAAC
NM_175920.3:c.819-415_819-413delinsAAC NP_787116.2:n.819-415_819-413delinsAAC
XM_024446045.1:c.861-415_861-413delinsAAC XP_024301813.1:n.861-415_861-413delinsAAC
NM_005575.3:c.861-415_861-413delinsAAC MANE Select NP_005566.2:n.861-415_861-413delinsAAC
NM_175920.4:c.819-415_819-413delinsAAC NP_787116.2:n.819-415_819-413delinsAAC