Canonical Allele Identifier: CA349695359
Gene: LNPK HGNC NCBI
ClinVar RCV:
ClinVar Variation:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.175964586C>A , CM000664.2:g.175964586C>A GRCh38
NC_000002.11:g.176829314C>A , CM000664.1:g.176829314C>A GRCh37
NC_000002.10:g.176537560C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272748.9:c.361G>T MANE Select ENSP00000272748.4:p.Glu121Ter
ENST00000272748.8:c.361G>T ENSP00000272748.4:p.Glu121Ter
ENST00000409660.5:c.-9G>T ENSP00000386237.1:n.-9G>T
ENST00000544803.5:c.361G>T ENSP00000440905.1:p.Glu121Ter
NM_001305008.1:c.559G>T NP_001291937.1:p.Glu187Ter
NM_001305009.1:c.361G>T NP_001291938.1:p.Glu121Ter
NM_001305010.1:c.367G>T NP_001291939.1:p.Glu123Ter
NM_001305011.1:c.-9G>T NP_001291940.1:n.-9G>T
NM_030650.2:c.361G>T NP_085153.1:p.Glu121Ter
NR_130941.1:n.898G>T
XM_005246878.2:c.361G>T XP_005246935.1:p.Glu121Ter
XM_005246879.3:c.136G>T XP_005246936.1:p.Glu46Ter
XM_005246880.3:c.7G>T XP_005246937.1:p.Glu3Ter
XM_006712783.2:c.361G>T XP_006712846.1:p.Glu121Ter
XM_011511945.1:c.136G>T XP_011510247.1:p.Glu46Ter
XM_005246878.4:c.361G>T XP_005246935.1:p.Glu121Ter
XM_005246879.4:c.136G>T XP_005246936.1:p.Glu46Ter
XM_011511945.2:c.136G>T XP_011510247.1:p.Glu46Ter
XM_017005055.1:c.-9G>T XP_016860544.1:n.-9G>T
NM_030650.3:c.361G>T MANE Select NP_085153.1:p.Glu121Ter
NM_001305011.2:c.-9G>T NP_001291940.1:n.-9G>T
NR_130941.2:n.879G>T