Canonical Allele Identifier: CA1200112245
Gene: PKLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155294653G= , CM000663.2:g.155294653G= GRCh38
NC_000001.10:g.155264444G= , CM000663.1:g.155264444G= GRCh37
NC_000001.9:g.153531068G= NCBI36
NG_011677.1:g.11782C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342741.6:c.794C= MANE Select ENSP00000339933.4:p.Ser265=
ENST00000342741.4:c.794C= ENSP00000339933.4:p.Ser265=
ENST00000392414.7:c.701C= ENSP00000376214.3:p.Ser234=
NM_000298.5:c.794C= NP_000289.1:p.Ser265=
NM_181871.3:c.701C= NP_870986.1:p.Ser234=
XM_005245266.3:c.953C= XP_005245323.1:p.Ser318=
XM_006711386.2:c.602C= XP_006711449.1:p.Ser201=
XM_011509639.1:c.953C= XP_011507941.1:p.Ser318=
XM_011509640.1:c.602C= XP_011507942.1:p.Ser201=
NM_000298.6:c.794C= MANE Select NP_000289.1:p.Ser265=
XM_006711386.4:c.602C= XP_006711449.1:p.Ser201=
XM_011509640.3:c.602C= XP_011507942.1:p.Ser201=
XM_017001493.1:c.794C= XP_016856982.1:p.Ser265=
NM_181871.4:c.701C= NP_870986.1:p.Ser234=