Canonical Allele Identifier: CA2674699051

Gene: LNPEP

Linked Data

• gnomAD v4: 5-97015049-ACCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.97015053_97015055del , CM000667.2:g.97015053_97015055del	GRCh38
NC_000005.9:g.96350757_96350759del , CM000667.1:g.96350757_96350759del	GRCh37
NC_000005.8:g.96376513_96376515del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231368.10:c.2334_2336del MANE Select	ENSP00000231368.5:p.Leu779del
ENST00000231368.9:c.2334_2336del	ENSP00000231368.5:p.Leu779del
ENST00000395770.3:c.2292_2294del	ENSP00000379117.3:p.Leu765del
NM_005575.2:c.2334_2336del	NP_005566.2:p.Leu779del
NM_175920.3:c.2292_2294del	NP_787116.2:p.Leu765del
XM_024446045.1:c.2334_2336del	XP_024301813.1:p.Leu779del
NM_005575.3:c.2334_2336del MANE Select	NP_005566.2:p.Leu779del
NM_175920.4:c.2292_2294del	NP_787116.2:p.Leu765del