Canonical Allele Identifier: CA2481224825
Gene: PKLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155290664A= , CM000663.2:g.155290664A= GRCh38
NC_000001.10:g.155260455A= , CM000663.1:g.155260455A= GRCh37
NC_000001.9:g.153527079A= NCBI36
NG_011677.1:g.15771T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342741.6:c.1633T= MANE Select ENSP00000339933.4:p.Phe545=
ENST00000342741.4:c.1633T= ENSP00000339933.4:p.Phe545=
ENST00000392414.7:c.1540T= ENSP00000376214.3:p.Phe514=
NM_000298.5:c.1633T= NP_000289.1:p.Phe545=
NM_181871.3:c.1540T= NP_870986.1:p.Phe514=
XM_005245266.3:c.1792T= XP_005245323.1:p.Phe598=
XM_006711386.2:c.1441T= XP_006711449.1:p.Phe481=
XM_011509640.1:c.1441T= XP_011507942.1:p.Phe481=
NM_000298.6:c.1633T= MANE Select NP_000289.1:p.Phe545=
XM_006711386.4:c.1441T= XP_006711449.1:p.Phe481=
XM_011509640.3:c.1441T= XP_011507942.1:p.Phe481=
NM_181871.4:c.1540T= NP_870986.1:p.Phe514=