Canonical Allele Identifier: CA445518227
Gene: LNPEP HGNC NCBI

Linked Data

gnomAD v4: 5-97015011-C-A
MyVariant Identifiers: chr5:g.96350715C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.97015011C>A , CM000667.2:g.97015011C>A GRCh38
NC_000005.9:g.96350715C>A , CM000667.1:g.96350715C>A GRCh37
NC_000005.8:g.96376471C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000231368.10:c.2292C>A MANE Select ENSP00000231368.5:p.Pro764=
ENST00000231368.9:c.2292C>A ENSP00000231368.5:p.Pro764=
ENST00000395770.3:c.2250C>A ENSP00000379117.3:p.Pro750=
NM_005575.2:c.2292C>A NP_005566.2:p.Pro764=
NM_175920.3:c.2250C>A NP_787116.2:p.Pro750=
XM_024446045.1:c.2292C>A XP_024301813.1:p.Pro764=
NM_005575.3:c.2292C>A MANE Select NP_005566.2:p.Pro764=
NM_175920.4:c.2250C>A NP_787116.2:p.Pro750=
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