Canonical Allele Identifier: CA2674699031
Gene: LNPEP HGNC NCBI

Linked Data

gnomAD v4: 5-97014925-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.97014929del , CM000667.2:g.97014929del GRCh38
NC_000005.9:g.96350633del , CM000667.1:g.96350633del GRCh37
NC_000005.8:g.96376389del NCBI36

Transcript Alleles

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