Canonical Allele Identifier: CA445518210
Gene: LNPEP HGNC NCBI

Linked Data

gnomAD v4: 5-97015005-T-C
MyVariant Identifiers: chr5:g.96350709T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.97015005T>C , CM000667.2:g.97015005T>C GRCh38
NC_000005.9:g.96350709T>C , CM000667.1:g.96350709T>C GRCh37
NC_000005.8:g.96376465T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000231368.10:c.2286T>C MANE Select ENSP00000231368.5:p.Thr762=
ENST00000231368.9:c.2286T>C ENSP00000231368.5:p.Thr762=
ENST00000395770.3:c.2244T>C ENSP00000379117.3:p.Thr748=
NM_005575.2:c.2286T>C NP_005566.2:p.Thr762=
NM_175920.3:c.2244T>C NP_787116.2:p.Thr748=
XM_024446045.1:c.2286T>C XP_024301813.1:p.Thr762=
NM_005575.3:c.2286T>C MANE Select NP_005566.2:p.Thr762=
NM_175920.4:c.2244T>C NP_787116.2:p.Thr748=
Search 100 bp 5'
Search 100 bp 3'