Canonical Allele Identifier: CA2674699070

Gene: LNPEP

Linked Data

• gnomAD v4: 5-97015116-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.97015116G>T , CM000667.2:g.97015116G>T	GRCh38
NC_000005.9:g.96350820G>T , CM000667.1:g.96350820G>T	GRCh37
NC_000005.8:g.96376576G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231368.10:c.2376+21G>T MANE Select	ENSP00000231368.5:n.2376+21G>T
ENST00000231368.9:c.2376+21G>T	ENSP00000231368.5:n.2376+21G>T
ENST00000395770.3:c.2334+21G>T	ENSP00000379117.3:n.2334+21G>T
NM_005575.2:c.2376+21G>T	NP_005566.2:n.2376+21G>T
NM_175920.3:c.2334+21G>T	NP_787116.2:n.2334+21G>T
XM_024446045.1:c.2376+21G>T	XP_024301813.1:n.2376+21G>T
NM_005575.3:c.2376+21G>T MANE Select	NP_005566.2:n.2376+21G>T
NM_175920.4:c.2334+21G>T	NP_787116.2:n.2334+21G>T