Canonical Allele Identifier: CA1565667941
Gene: LNPEP HGNC NCBI

Linked Data

dbSNP Id: rs1790203102
gnomAD v3: 5-96984763-T-G
gnomAD v4: 5-96984763-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96984763T>G , CM000667.2:g.96984763T>G GRCh38
NC_000005.9:g.96320467T>G , CM000667.1:g.96320467T>G GRCh37
NC_000005.8:g.96346223T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000231368.10:c.861-317T>G MANE Select ENSP00000231368.5:n.861-317T>G
ENST00000231368.9:c.861-317T>G ENSP00000231368.5:n.861-317T>G
ENST00000395770.3:c.819-317T>G ENSP00000379117.3:n.819-317T>G
NM_005575.2:c.861-317T>G NP_005566.2:n.861-317T>G
NM_175920.3:c.819-317T>G NP_787116.2:n.819-317T>G
XM_024446045.1:c.861-317T>G XP_024301813.1:n.861-317T>G
NM_005575.3:c.861-317T>G MANE Select NP_005566.2:n.861-317T>G
NM_175920.4:c.819-317T>G NP_787116.2:n.819-317T>G
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