Canonical Allele Identifier: CA2674699049

Gene: LNPEP

Linked Data

• gnomAD v4: 5-97015013-TCACC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.97015014_97015017del , CM000667.2:g.97015014_97015017del	GRCh38
NC_000005.9:g.96350718_96350721del , CM000667.1:g.96350718_96350721del	GRCh37
NC_000005.8:g.96376474_96376477del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000231368.10:c.2295_2298del MANE Select	ENSP00000231368.5:p.Ile765MetfsTer27
ENST00000231368.9:c.2295_2298del	ENSP00000231368.5:p.Ile765MetfsTer27
ENST00000395770.3:c.2253_2256del	ENSP00000379117.3:p.Ile751MetfsTer27
NM_005575.2:c.2295_2298del	NP_005566.2:p.Ile765MetfsTer27
NM_175920.3:c.2253_2256del	NP_787116.2:p.Ile751MetfsTer27
XM_024446045.1:c.2295_2298del	XP_024301813.1:p.Ile765MetfsTer27
NM_005575.3:c.2295_2298del MANE Select	NP_005566.2:p.Ile765MetfsTer27
NM_175920.4:c.2253_2256del	NP_787116.2:p.Ile751MetfsTer27