Canonical Allele Identifier: CA360508539
Gene: LNPEP HGNC NCBI

Linked Data

gnomAD v4: 5-97015082-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.97015082C>A , CM000667.2:g.97015082C>A GRCh38
NC_000005.9:g.96350786C>A , CM000667.1:g.96350786C>A GRCh37
NC_000005.8:g.96376542C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000231368.10:c.2363C>A MANE Select ENSP00000231368.5:p.Ala788Asp
ENST00000231368.9:c.2363C>A ENSP00000231368.5:p.Ala788Asp
ENST00000395770.3:c.2321C>A ENSP00000379117.3:p.Ala774Asp
NM_005575.2:c.2363C>A NP_005566.2:p.Ala788Asp
NM_175920.3:c.2321C>A NP_787116.2:p.Ala774Asp
XM_024446045.1:c.2363C>A XP_024301813.1:p.Ala788Asp
NM_005575.3:c.2363C>A MANE Select NP_005566.2:p.Ala788Asp
NM_175920.4:c.2321C>A NP_787116.2:p.Ala774Asp