Canonical Allele Identifier: CA1200112280
Gene: PKLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155294731T= , CM000663.2:g.155294731T= GRCh38
NC_000001.10:g.155264522T= , CM000663.1:g.155264522T= GRCh37
NC_000001.9:g.153531146T= NCBI36
NG_011677.1:g.11704A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342741.6:c.716A= MANE Select ENSP00000339933.4:p.Gln239=
ENST00000342741.4:c.716A= ENSP00000339933.4:p.Gln239=
ENST00000392414.7:c.623A= ENSP00000376214.3:p.Gln208=
NM_000298.5:c.716A= NP_000289.1:p.Gln239=
NM_181871.3:c.623A= NP_870986.1:p.Gln208=
XM_005245266.3:c.875A= XP_005245323.1:p.Gln292=
XM_006711386.2:c.524A= XP_006711449.1:p.Gln175=
XM_011509639.1:c.875A= XP_011507941.1:p.Gln292=
XM_011509640.1:c.524A= XP_011507942.1:p.Gln175=
NM_000298.6:c.716A= MANE Select NP_000289.1:p.Gln239=
XM_006711386.4:c.524A= XP_006711449.1:p.Gln175=
XM_011509640.3:c.524A= XP_011507942.1:p.Gln175=
XM_017001493.1:c.716A= XP_016856982.1:p.Gln239=
NM_181871.4:c.623A= NP_870986.1:p.Gln208=