Canonical Allele Identifier: CA3354211
Gene: LNPEP HGNC NCBI

Linked Data

dbSNP Id: rs761457107
ExAC: 5:96350721 C / T
gnomAD v2: 5-96350721-C-T
gnomAD v4: 5-97015017-C-T
MyVariant Identifiers: chr5:g.96350721C>T (hg19) chr5:g.97015017C>T (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000231368.10:c.2298C>T MANE Select ENSP00000231368.5:p.Thr766=
ENST00000231368.9:c.2298C>T ENSP00000231368.5:p.Thr766=
ENST00000395770.3:c.2256C>T ENSP00000379117.3:p.Thr752=
NM_005575.2:c.2298C>T NP_005566.2:p.Thr766=
NM_175920.3:c.2256C>T NP_787116.2:p.Thr752=
XM_024446045.1:c.2298C>T XP_024301813.1:p.Thr766=
NM_005575.3:c.2298C>T MANE Select NP_005566.2:p.Thr766=
NM_175920.4:c.2256C>T NP_787116.2:p.Thr752=
Search 100 bp 5'
Search 100 bp 3'