Canonical Allele Identifier: CA445518242
Gene: LNPEP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.96350721C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.97015017C>A , CM000667.2:g.97015017C>A GRCh38
NC_000005.9:g.96350721C>A , CM000667.1:g.96350721C>A GRCh37
NC_000005.8:g.96376477C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000231368.10:c.2298C>A MANE Select ENSP00000231368.5:p.Thr766=
ENST00000231368.9:c.2298C>A ENSP00000231368.5:p.Thr766=
ENST00000395770.3:c.2256C>A ENSP00000379117.3:p.Thr752=
NM_005575.2:c.2298C>A NP_005566.2:p.Thr766=
NM_175920.3:c.2256C>A NP_787116.2:p.Thr752=
XM_024446045.1:c.2298C>A XP_024301813.1:p.Thr766=
NM_005575.3:c.2298C>A MANE Select NP_005566.2:p.Thr766=
NM_175920.4:c.2256C>A NP_787116.2:p.Thr752=
Search 100 bp 5'
Search 100 bp 3'