Canonical Allele Identifier: CA2481225426
Gene: PKLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155291883G= , CM000663.2:g.155291883G= GRCh38
NC_000001.10:g.155261674G= , CM000663.1:g.155261674G= GRCh37
NC_000001.9:g.153528298G= NCBI36
NG_011677.1:g.14552C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342741.6:c.1491C= MANE Select ENSP00000339933.4:p.Thr497=
ENST00000342741.4:c.1491C= ENSP00000339933.4:p.Thr497=
ENST00000392414.7:c.1398C= ENSP00000376214.3:p.Thr466=
NM_000298.5:c.1491C= NP_000289.1:p.Thr497=
NM_181871.3:c.1398C= NP_870986.1:p.Thr466=
XM_005245266.3:c.1650C= XP_005245323.1:p.Thr550=
XM_006711386.2:c.1299C= XP_006711449.1:p.Thr433=
XM_011509640.1:c.1299C= XP_011507942.1:p.Thr433=
NM_000298.6:c.1491C= MANE Select NP_000289.1:p.Thr497=
XM_006711386.4:c.1299C= XP_006711449.1:p.Thr433=
XM_011509640.3:c.1299C= XP_011507942.1:p.Thr433=
NM_181871.4:c.1398C= NP_870986.1:p.Thr466=