Canonical Allele Identifier: CA122979039
Gene: LNPEP HGNC NCBI

Linked Data

dbSNP Id: rs199528485
gnomAD v2: 5-96320508-C-G
gnomAD v3: 5-96984804-C-G
gnomAD v4: 5-96984804-C-G
MyVariant Identifiers: chr5:g.96320508C>G (hg19) chr5:g.96984804C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96984804C>G , CM000667.2:g.96984804C>G GRCh38
NC_000005.9:g.96320508C>G , CM000667.1:g.96320508C>G GRCh37
NC_000005.8:g.96346264C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000231368.10:c.861-276C>G MANE Select ENSP00000231368.5:n.861-276C>G
ENST00000231368.9:c.861-276C>G ENSP00000231368.5:n.861-276C>G
ENST00000395770.3:c.819-276C>G ENSP00000379117.3:n.819-276C>G
NM_005575.2:c.861-276C>G NP_005566.2:n.861-276C>G
NM_175920.3:c.819-276C>G NP_787116.2:n.819-276C>G
XM_024446045.1:c.861-276C>G XP_024301813.1:n.861-276C>G
NM_005575.3:c.861-276C>G MANE Select NP_005566.2:n.861-276C>G
NM_175920.4:c.819-276C>G NP_787116.2:n.819-276C>G
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