Canonical Allele Identifier: CA360508212
Gene: LNPEP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.96350736G>C (hg19) chr5:g.97015032G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.97015032G>C , CM000667.2:g.97015032G>C GRCh38
NC_000005.9:g.96350736G>C , CM000667.1:g.96350736G>C GRCh37
NC_000005.8:g.96376492G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000231368.10:c.2313G>C MANE Select ENSP00000231368.5:p.Gln771His
ENST00000231368.9:c.2313G>C ENSP00000231368.5:p.Gln771His
ENST00000395770.3:c.2271G>C ENSP00000379117.3:p.Gln757His
NM_005575.2:c.2313G>C NP_005566.2:p.Gln771His
NM_175920.3:c.2271G>C NP_787116.2:p.Gln757His
XM_024446045.1:c.2313G>C XP_024301813.1:p.Gln771His
NM_005575.3:c.2313G>C MANE Select NP_005566.2:p.Gln771His
NM_175920.4:c.2271G>C NP_787116.2:p.Gln757His
Search 100 bp 5'
Search 100 bp 3'