Canonical Allele Identifier: CA1200112237
Gene: PKLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155294638C= , CM000663.2:g.155294638C= GRCh38
NC_000001.10:g.155264429C= , CM000663.1:g.155264429C= GRCh37
NC_000001.9:g.153531053C= NCBI36
NG_011677.1:g.11797G=

Transcript Alleles

HGVS Amino-acid change
ENST00000342741.6:c.809G= MANE Select ENSP00000339933.4:p.Arg270=
ENST00000342741.4:c.809G= ENSP00000339933.4:p.Arg270=
ENST00000392414.7:c.716G= ENSP00000376214.3:p.Arg239=
NM_000298.5:c.809G= NP_000289.1:p.Arg270=
NM_181871.3:c.716G= NP_870986.1:p.Arg239=
XM_005245266.3:c.968G= XP_005245323.1:p.Arg323=
XM_006711386.2:c.617G= XP_006711449.1:p.Arg206=
XM_011509639.1:c.968G= XP_011507941.1:p.Arg323=
XM_011509640.1:c.617G= XP_011507942.1:p.Arg206=
NM_000298.6:c.809G= MANE Select NP_000289.1:p.Arg270=
XM_006711386.4:c.617G= XP_006711449.1:p.Arg206=
XM_011509640.3:c.617G= XP_011507942.1:p.Arg206=
XM_017001493.1:c.809G= XP_016856982.1:p.Arg270=
NM_181871.4:c.716G= NP_870986.1:p.Arg239=