Canonical Allele Identifier: CA360508533
Gene: LNPEP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.97015081G>C , CM000667.2:g.97015081G>C GRCh38
NC_000005.9:g.96350785G>C , CM000667.1:g.96350785G>C GRCh37
NC_000005.8:g.96376541G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000231368.10:c.2362G>C MANE Select ENSP00000231368.5:p.Ala788Pro
ENST00000231368.9:c.2362G>C ENSP00000231368.5:p.Ala788Pro
ENST00000395770.3:c.2320G>C ENSP00000379117.3:p.Ala774Pro
NM_005575.2:c.2362G>C NP_005566.2:p.Ala788Pro
NM_175920.3:c.2320G>C NP_787116.2:p.Ala774Pro
XM_024446045.1:c.2362G>C XP_024301813.1:p.Ala788Pro
NM_005575.3:c.2362G>C MANE Select NP_005566.2:p.Ala788Pro
NM_175920.4:c.2320G>C NP_787116.2:p.Ala774Pro