Canonical Allele Identifier: CA122979033

Gene: LNPEP

Linked Data

• dbSNP Id: rs776851942
• MyVariant Identifiers: chr5:g.96320498C>G (hg19) ; chr5:g.96984794C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96984794C>G , CM000667.2:g.96984794C>G	GRCh38
NC_000005.9:g.96320498C>G , CM000667.1:g.96320498C>G	GRCh37
NC_000005.8:g.96346254C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231368.10:c.861-286C>G MANE Select	ENSP00000231368.5:n.861-286C>G
ENST00000231368.9:c.861-286C>G	ENSP00000231368.5:n.861-286C>G
ENST00000395770.3:c.819-286C>G	ENSP00000379117.3:n.819-286C>G
NM_005575.2:c.861-286C>G	NP_005566.2:n.861-286C>G
NM_175920.3:c.819-286C>G	NP_787116.2:n.819-286C>G
XM_024446045.1:c.861-286C>G	XP_024301813.1:n.861-286C>G
NM_005575.3:c.861-286C>G MANE Select	NP_005566.2:n.861-286C>G
NM_175920.4:c.819-286C>G	NP_787116.2:n.819-286C>G