Canonical Allele Identifier: CA1565667933
Gene: LNPEP HGNC NCBI

Linked Data

dbSNP Id: rs1289467375
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96984752A>T , CM000667.2:g.96984752A>T GRCh38
NC_000005.9:g.96320456A>T , CM000667.1:g.96320456A>T GRCh37
NC_000005.8:g.96346212A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000231368.10:c.861-328A>T MANE Select ENSP00000231368.5:n.861-328A>T
ENST00000231368.9:c.861-328A>T ENSP00000231368.5:n.861-328A>T
ENST00000395770.3:c.819-328A>T ENSP00000379117.3:n.819-328A>T
NM_005575.2:c.861-328A>T NP_005566.2:n.861-328A>T
NM_175920.3:c.819-328A>T NP_787116.2:n.819-328A>T
XM_024446045.1:c.861-328A>T XP_024301813.1:n.861-328A>T
NM_005575.3:c.861-328A>T MANE Select NP_005566.2:n.861-328A>T
NM_175920.4:c.819-328A>T NP_787116.2:n.819-328A>T
Search 100 bp 5'
Search 100 bp 3'