Canonical Allele Identifier: CA1565681257

Gene: LNPEP

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.97015072A= , CM000667.2:g.97015072A=	GRCh38
NC_000005.9:g.96350776A= , CM000667.1:g.96350776A=	GRCh37
NC_000005.8:g.96376532A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231368.10:c.2353A= MANE Select	ENSP00000231368.5:p.Met785=
ENST00000231368.9:c.2353A=	ENSP00000231368.5:p.Met785=
ENST00000395770.3:c.2311A=	ENSP00000379117.3:p.Met771=
NM_005575.2:c.2353A=	NP_005566.2:p.Met785=
NM_175920.3:c.2311A=	NP_787116.2:p.Met771=
XM_024446045.1:c.2353A=	XP_024301813.1:p.Met785=
NM_005575.3:c.2353A= MANE Select	NP_005566.2:p.Met785=
NM_175920.4:c.2311A=	NP_787116.2:p.Met771=