Canonical Allele Identifier: CA122978941

Gene: LNPEP

Linked Data

• dbSNP Id: rs551111525
• gnomAD v3: 5-96984727-C-T
• gnomAD v4: 5-96984727-C-T
• MyVariant Identifiers: chr5:g.96320431C>T (hg19) ; chr5:g.96984727C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96984727C>T , CM000667.2:g.96984727C>T	GRCh38
NC_000005.9:g.96320431C>T , CM000667.1:g.96320431C>T	GRCh37
NC_000005.8:g.96346187C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000231368.10:c.861-353C>T MANE Select	ENSP00000231368.5:n.861-353C>T
ENST00000231368.9:c.861-353C>T	ENSP00000231368.5:n.861-353C>T
ENST00000395770.3:c.819-353C>T	ENSP00000379117.3:n.819-353C>T
NM_005575.2:c.861-353C>T	NP_005566.2:n.861-353C>T
NM_175920.3:c.819-353C>T	NP_787116.2:n.819-353C>T
XM_024446045.1:c.861-353C>T	XP_024301813.1:n.861-353C>T
NM_005575.3:c.861-353C>T MANE Select	NP_005566.2:n.861-353C>T
NM_175920.4:c.819-353C>T	NP_787116.2:n.819-353C>T