Canonical Allele Identifier: CA815901216
Gene: LNPEP HGNC NCBI

Linked Data

dbSNP Id: rs1385895475
MyVariant Identifiers: chr5:g.96320450C>G (hg19) chr5:g.96984746C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96984746C>G , CM000667.2:g.96984746C>G GRCh38
NC_000005.9:g.96320450C>G , CM000667.1:g.96320450C>G GRCh37
NC_000005.8:g.96346206C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000231368.10:c.861-334C>G MANE Select ENSP00000231368.5:n.861-334C>G
ENST00000231368.9:c.861-334C>G ENSP00000231368.5:n.861-334C>G
ENST00000395770.3:c.819-334C>G ENSP00000379117.3:n.819-334C>G
NM_005575.2:c.861-334C>G NP_005566.2:n.861-334C>G
NM_175920.3:c.819-334C>G NP_787116.2:n.819-334C>G
XM_024446045.1:c.861-334C>G XP_024301813.1:n.861-334C>G
NM_005575.3:c.861-334C>G MANE Select NP_005566.2:n.861-334C>G
NM_175920.4:c.819-334C>G NP_787116.2:n.819-334C>G
Search 100 bp 5'
Search 100 bp 3'