Canonical Allele Identifier: CA2481224829
Gene: PKLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155290669C= , CM000663.2:g.155290669C= GRCh38
NC_000001.10:g.155260460C= , CM000663.1:g.155260460C= GRCh37
NC_000001.9:g.153527084C= NCBI36
NG_011677.1:g.15766G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342741.6:c.1628G= MANE Select ENSP00000339933.4:p.Arg543=
ENST00000342741.4:c.1628G= ENSP00000339933.4:p.Arg543=
ENST00000392414.7:c.1535G= ENSP00000376214.3:p.Arg512=
NM_000298.5:c.1628G= NP_000289.1:p.Arg543=
NM_181871.3:c.1535G= NP_870986.1:p.Arg512=
XM_005245266.3:c.1787G= XP_005245323.1:p.Arg596=
XM_006711386.2:c.1436G= XP_006711449.1:p.Arg479=
XM_011509640.1:c.1436G= XP_011507942.1:p.Arg479=
NM_000298.6:c.1628G= MANE Select NP_000289.1:p.Arg543=
XM_006711386.4:c.1436G= XP_006711449.1:p.Arg479=
XM_011509640.3:c.1436G= XP_011507942.1:p.Arg479=
NM_181871.4:c.1535G= NP_870986.1:p.Arg512=