Canonical Allele Identifier: CA1200112235
Gene: PKLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155294632A= , CM000663.2:g.155294632A= GRCh38
NC_000001.10:g.155264423A= , CM000663.1:g.155264423A= GRCh37
NC_000001.9:g.153531047A= NCBI36
NG_011677.1:g.11803T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342741.6:c.815T= MANE Select ENSP00000339933.4:p.Leu272=
ENST00000342741.4:c.815T= ENSP00000339933.4:p.Leu272=
ENST00000392414.7:c.722T= ENSP00000376214.3:p.Leu241=
NM_000298.5:c.815T= NP_000289.1:p.Leu272=
NM_181871.3:c.722T= NP_870986.1:p.Leu241=
XM_005245266.3:c.974T= XP_005245323.1:p.Leu325=
XM_006711386.2:c.623T= XP_006711449.1:p.Leu208=
XM_011509639.1:c.974T= XP_011507941.1:p.Leu325=
XM_011509640.1:c.623T= XP_011507942.1:p.Leu208=
NM_000298.6:c.815T= MANE Select NP_000289.1:p.Leu272=
XM_006711386.4:c.623T= XP_006711449.1:p.Leu208=
XM_011509640.3:c.623T= XP_011507942.1:p.Leu208=
XM_017001493.1:c.815T= XP_016856982.1:p.Leu272=
NM_181871.4:c.722T= NP_870986.1:p.Leu241=