Canonical Allele Identifier: CA445518229

Gene: LNPEP

Linked Data

• gnomAD v4: 5-97015011-C-T
• MyVariant Identifiers: chr5:g.96350715C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.97015011C>T , CM000667.2:g.97015011C>T	GRCh38
NC_000005.9:g.96350715C>T , CM000667.1:g.96350715C>T	GRCh37
NC_000005.8:g.96376471C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000231368.10:c.2292C>T MANE Select	ENSP00000231368.5:p.Pro764=
ENST00000231368.9:c.2292C>T	ENSP00000231368.5:p.Pro764=
ENST00000395770.3:c.2250C>T	ENSP00000379117.3:p.Pro750=
NM_005575.2:c.2292C>T	NP_005566.2:p.Pro764=
NM_175920.3:c.2250C>T	NP_787116.2:p.Pro750=
XM_024446045.1:c.2292C>T	XP_024301813.1:p.Pro764=
NM_005575.3:c.2292C>T MANE Select	NP_005566.2:p.Pro764=
NM_175920.4:c.2250C>T	NP_787116.2:p.Pro750=