Canonical Allele Identifier: CA360508135

Gene: LNPEP

Linked Data

• MyVariant Identifiers: chr5:g.96350719A>T (hg19) ; chr5:g.97015015A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.97015015A>T , CM000667.2:g.97015015A>T	GRCh38
NC_000005.9:g.96350719A>T , CM000667.1:g.96350719A>T	GRCh37
NC_000005.8:g.96376475A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000231368.10:c.2296A>T MANE Select	ENSP00000231368.5:p.Thr766Ser
ENST00000231368.9:c.2296A>T	ENSP00000231368.5:p.Thr766Ser
ENST00000395770.3:c.2254A>T	ENSP00000379117.3:p.Thr752Ser
NM_005575.2:c.2296A>T	NP_005566.2:p.Thr766Ser
NM_175920.3:c.2254A>T	NP_787116.2:p.Thr752Ser
XM_024446045.1:c.2296A>T	XP_024301813.1:p.Thr766Ser
NM_005575.3:c.2296A>T MANE Select	NP_005566.2:p.Thr766Ser
NM_175920.4:c.2254A>T	NP_787116.2:p.Thr752Ser