Canonical Allele Identifier: CA360508095

Gene: LNPEP

Linked Data

• MyVariant Identifiers: chr5:g.96350710G>T (hg19) ; chr5:g.97015006G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.97015006G>T , CM000667.2:g.97015006G>T	GRCh38
NC_000005.9:g.96350710G>T , CM000667.1:g.96350710G>T	GRCh37
NC_000005.8:g.96376466G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000231368.10:c.2287G>T MANE Select	ENSP00000231368.5:p.Ala763Ser
ENST00000231368.9:c.2287G>T	ENSP00000231368.5:p.Ala763Ser
ENST00000395770.3:c.2245G>T	ENSP00000379117.3:p.Ala749Ser
NM_005575.2:c.2287G>T	NP_005566.2:p.Ala763Ser
NM_175920.3:c.2245G>T	NP_787116.2:p.Ala749Ser
XM_024446045.1:c.2287G>T	XP_024301813.1:p.Ala763Ser
NM_005575.3:c.2287G>T MANE Select	NP_005566.2:p.Ala763Ser
NM_175920.4:c.2245G>T	NP_787116.2:p.Ala749Ser