Canonical Allele Identifier: CA1141653696
Gene: PKLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155291822G= , CM000663.2:g.155291822G= GRCh38
NC_000001.10:g.155261613G= , CM000663.1:g.155261613G= GRCh37
NC_000001.9:g.153528237G= NCBI36
NG_011677.1:g.14613C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342741.6:c.1552C= MANE Select ENSP00000339933.4:p.Arg518=
ENST00000342741.4:c.1552C= ENSP00000339933.4:p.Arg518=
ENST00000392414.7:c.1459C= ENSP00000376214.3:p.Arg487=
NM_000298.5:c.1552C= NP_000289.1:p.Arg518=
NM_181871.3:c.1459C= NP_870986.1:p.Arg487=
XM_005245266.3:c.1711C= XP_005245323.1:p.Arg571=
XM_006711386.2:c.1360C= XP_006711449.1:p.Arg454=
XM_011509640.1:c.1360C= XP_011507942.1:p.Arg454=
NM_000298.6:c.1552C= MANE Select NP_000289.1:p.Arg518=
XM_006711386.4:c.1360C= XP_006711449.1:p.Arg454=
XM_011509640.3:c.1360C= XP_011507942.1:p.Arg454=
NM_181871.4:c.1459C= NP_870986.1:p.Arg487=