Canonical Allele Identifier: CA1200112196
Gene: PKLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155294511G= , CM000663.2:g.155294511G= GRCh38
NC_000001.10:g.155264302G= , CM000663.1:g.155264302G= GRCh37
NC_000001.9:g.153530926G= NCBI36
NG_011677.1:g.11924C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342741.6:c.936C= MANE Select ENSP00000339933.4:p.Ser312=
ENST00000342741.4:c.936C= ENSP00000339933.4:p.Ser312=
ENST00000392414.7:c.843C= ENSP00000376214.3:p.Ser281=
NM_000298.5:c.936C= NP_000289.1:p.Ser312=
NM_181871.3:c.843C= NP_870986.1:p.Ser281=
XM_005245266.3:c.1095C= XP_005245323.1:p.Ser365=
XM_006711386.2:c.744C= XP_006711449.1:p.Ser248=
XM_011509639.1:c.1095C= XP_011507941.1:p.Ser365=
XM_011509640.1:c.744C= XP_011507942.1:p.Ser248=
NM_000298.6:c.936C= MANE Select NP_000289.1:p.Ser312=
XM_006711386.4:c.744C= XP_006711449.1:p.Ser248=
XM_011509640.3:c.744C= XP_011507942.1:p.Ser248=
XM_017001493.1:c.936C= XP_016856982.1:p.Ser312=
NM_181871.4:c.843C= NP_870986.1:p.Ser281=