Canonical Allele Identifier: CA445518327

Gene: LNPEP

Linked Data

• MyVariant Identifiers: chr5:g.96350745C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.97015041C>A , CM000667.2:g.97015041C>A	GRCh38
NC_000005.9:g.96350745C>A , CM000667.1:g.96350745C>A	GRCh37
NC_000005.8:g.96376501C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231368.10:c.2322C>A MANE Select	ENSP00000231368.5:p.Leu774=
ENST00000231368.9:c.2322C>A	ENSP00000231368.5:p.Leu774=
ENST00000395770.3:c.2280C>A	ENSP00000379117.3:p.Leu760=
NM_005575.2:c.2322C>A	NP_005566.2:p.Leu774=
NM_175920.3:c.2280C>A	NP_787116.2:p.Leu760=
XM_024446045.1:c.2322C>A	XP_024301813.1:p.Leu774=
NM_005575.3:c.2322C>A MANE Select	NP_005566.2:p.Leu774=
NM_175920.4:c.2280C>A	NP_787116.2:p.Leu760=