Canonical Allele Identifier: CA360508398

Gene: LNPEP

Linked Data

• MyVariant Identifiers: chr5:g.96350762A>T (hg19) ; chr5:g.97015058A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.97015058A>T , CM000667.2:g.97015058A>T	GRCh38
NC_000005.9:g.96350762A>T , CM000667.1:g.96350762A>T	GRCh37
NC_000005.8:g.96376518A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231368.10:c.2339A>T MANE Select	ENSP00000231368.5:p.Glu780Val
ENST00000231368.9:c.2339A>T	ENSP00000231368.5:p.Glu780Val
ENST00000395770.3:c.2297A>T	ENSP00000379117.3:p.Glu766Val
NM_005575.2:c.2339A>T	NP_005566.2:p.Glu780Val
NM_175920.3:c.2297A>T	NP_787116.2:p.Glu766Val
XM_024446045.1:c.2339A>T	XP_024301813.1:p.Glu780Val
NM_005575.3:c.2339A>T MANE Select	NP_005566.2:p.Glu780Val
NM_175920.4:c.2297A>T	NP_787116.2:p.Glu766Val