Canonical Allele Identifier: CA342753728
Gene: PKLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155294500T>A , CM000663.2:g.155294500T>A GRCh38
NC_000001.10:g.155264291T>A , CM000663.1:g.155264291T>A GRCh37
NC_000001.9:g.153530915T>A NCBI36
NG_011677.1:g.11935A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342741.6:c.947A>T MANE Select ENSP00000339933.4:p.Asn316Ile
ENST00000342741.4:c.947A>T ENSP00000339933.4:p.Asn316Ile
ENST00000392414.7:c.854A>T ENSP00000376214.3:p.Asn285Ile
NM_000298.5:c.947A>T NP_000289.1:p.Asn316Ile
NM_181871.3:c.854A>T NP_870986.1:p.Asn285Ile
XM_005245266.3:c.1106A>T XP_005245323.1:p.Asn369Ile
XM_006711386.2:c.755A>T XP_006711449.1:p.Asn252Ile
XM_011509639.1:c.1106A>T XP_011507941.1:p.Asn369Ile
XM_011509640.1:c.755A>T XP_011507942.1:p.Asn252Ile
NM_000298.6:c.947A>T MANE Select NP_000289.1:p.Asn316Ile
XM_006711386.4:c.755A>T XP_006711449.1:p.Asn252Ile
XM_011509640.3:c.755A>T XP_011507942.1:p.Asn252Ile
XM_017001493.1:c.947A>T XP_016856982.1:p.Asn316Ile
NM_181871.4:c.854A>T NP_870986.1:p.Asn285Ile