Canonical Allele Identifier: CA360508424

Gene: LNPEP

Linked Data

• MyVariant Identifiers: chr5:g.96350765A>T (hg19) ; chr5:g.97015061A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.97015061A>T , CM000667.2:g.97015061A>T	GRCh38
NC_000005.9:g.96350765A>T , CM000667.1:g.96350765A>T	GRCh37
NC_000005.8:g.96376521A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231368.10:c.2342A>T MANE Select	ENSP00000231368.5:p.Lys781Ile
ENST00000231368.9:c.2342A>T	ENSP00000231368.5:p.Lys781Ile
ENST00000395770.3:c.2300A>T	ENSP00000379117.3:p.Lys767Ile
NM_005575.2:c.2342A>T	NP_005566.2:p.Lys781Ile
NM_175920.3:c.2300A>T	NP_787116.2:p.Lys767Ile
XM_024446045.1:c.2342A>T	XP_024301813.1:p.Lys781Ile
NM_005575.3:c.2342A>T MANE Select	NP_005566.2:p.Lys781Ile
NM_175920.4:c.2300A>T	NP_787116.2:p.Lys767Ile