Canonical Allele Identifier: CA1144039
Community Standard Title: NM_000298.6(PKLR):c.1318G>T (p.Glu440Ter)
Gene: PKLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155293295C>A , CM000663.2:g.155293295C>A GRCh38
NC_000001.10:g.155263086C>A , CM000663.1:g.155263086C>A GRCh37
NC_000001.9:g.153529710C>A NCBI36
NG_011677.1:g.13140G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000298.6:c.1318G>T MANE Select NP_000289.1:p.Glu440Ter
ENST00000342741.6:c.1318G>T MANE Select ENSP00000339933.4:p.Glu440Ter
NM_000298.5:c.1318G>T NP_000289.1:p.Glu440Ter
NM_181871.3:c.1225G>T NP_870986.1:p.Glu409Ter
NM_181871.4:c.1225G>T NP_870986.1:p.Glu409Ter
ENST00000342741.4:c.1318G>T ENSP00000339933.4:p.Glu440Ter
ENST00000392414.7:c.1225G>T ENSP00000376214.3:p.Glu409Ter
XM_005245266.3:c.1477G>T XP_005245323.1:p.Glu493Ter
XM_006711386.2:c.1126G>T XP_006711449.1:p.Glu376Ter
XM_006711386.4:c.1126G>T XP_006711449.1:p.Glu376Ter
XM_011509640.1:c.1126G>T XP_011507942.1:p.Glu376Ter
XM_011509640.3:c.1126G>T XP_011507942.1:p.Glu376Ter