Canonical Allele Identifier: CA122979009
Gene: LNPEP HGNC NCBI

Linked Data

dbSNP Id: rs10044354

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96984791C>T , CM000667.2:g.96984791C>T GRCh38
NC_000005.9:g.96320495C>T , CM000667.1:g.96320495C>T GRCh37
NC_000005.8:g.96346251C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000231368.9:c.861-289C>T ENSP00000231368.5:p.=
ENST00000395770.3:c.819-289C>T ENSP00000379117.3:p.=
NM_005575.2:c.861-289C>T NP_005566.2:p.=
NM_175920.3:c.819-289C>T NP_787116.2:p.=
XM_024446045.1:c.861-289C>T XP_024301813.1:p.=
NM_005575.3:c.861-289C>T MANE Select NP_005566.2:p.=
NM_175920.4:c.819-289C>T NP_787116.2:p.=