Canonical Allele Identifier: CA2481224806
Gene: PKLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155290596G= , CM000663.2:g.155290596G= GRCh38
NC_000001.10:g.155260387G= , CM000663.1:g.155260387G= GRCh37
NC_000001.9:g.153527011G= NCBI36
NG_011677.1:g.15839C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342741.6:c.1701C= MANE Select ENSP00000339933.4:p.Ile567=
ENST00000342741.4:c.1701C= ENSP00000339933.4:p.Ile567=
ENST00000392414.7:c.1608C= ENSP00000376214.3:p.Ile536=
NM_000298.5:c.1701C= NP_000289.1:p.Ile567=
NM_181871.3:c.1608C= NP_870986.1:p.Ile536=
XM_005245266.3:c.1860C= XP_005245323.1:p.Ile620=
XM_006711386.2:c.1509C= XP_006711449.1:p.Ile503=
XM_011509640.1:c.1509C= XP_011507942.1:p.Ile503=
NM_000298.6:c.1701C= MANE Select NP_000289.1:p.Ile567=
XM_006711386.4:c.1509C= XP_006711449.1:p.Ile503=
XM_011509640.3:c.1509C= XP_011507942.1:p.Ile503=
NM_181871.4:c.1608C= NP_870986.1:p.Ile536=