Canonical Allele Identifier: CA1079064627
Gene: LNPEP HGNC NCBI

Linked Data

dbSNP Id: rs1790199791
gnomAD v3: 5-96984618-TA-T
gnomAD v4: 5-96984618-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96984621del , CM000667.2:g.96984621del GRCh38
NC_000005.9:g.96320325del , CM000667.1:g.96320325del GRCh37
NC_000005.8:g.96346081del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000231368.10:c.861-459del MANE Select ENSP00000231368.5:n.861-459del
ENST00000231368.9:c.861-459del ENSP00000231368.5:n.861-459del
ENST00000395770.3:c.819-459del ENSP00000379117.3:n.819-459del
NM_005575.2:c.861-459del NP_005566.2:n.861-459del
NM_175920.3:c.819-459del NP_787116.2:n.819-459del
XM_024446045.1:c.861-459del XP_024301813.1:n.861-459del
NM_005575.3:c.861-459del MANE Select NP_005566.2:n.861-459del
NM_175920.4:c.819-459del NP_787116.2:n.819-459del
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