Canonical Allele Identifier: CA2674699055

Gene: LNPEP

Linked Data

• gnomAD v4: 5-97015098-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.97015098A>G , CM000667.2:g.97015098A>G	GRCh38
NC_000005.9:g.96350802A>G , CM000667.1:g.96350802A>G	GRCh37
NC_000005.8:g.96376558A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231368.10:c.2376+3A>G MANE Select	ENSP00000231368.5:n.2376+3A>G
ENST00000231368.9:c.2376+3A>G	ENSP00000231368.5:n.2376+3A>G
ENST00000395770.3:c.2334+3A>G	ENSP00000379117.3:n.2334+3A>G
NM_005575.2:c.2376+3A>G	NP_005566.2:n.2376+3A>G
NM_175920.3:c.2334+3A>G	NP_787116.2:n.2334+3A>G
XM_024446045.1:c.2376+3A>G	XP_024301813.1:n.2376+3A>G
NM_005575.3:c.2376+3A>G MANE Select	NP_005566.2:n.2376+3A>G
NM_175920.4:c.2334+3A>G	NP_787116.2:n.2334+3A>G