Canonical Allele Identifier: CA342753588
Gene: PKLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155294383A>C , CM000663.2:g.155294383A>C GRCh38
NC_000001.10:g.155264174A>C , CM000663.1:g.155264174A>C GRCh37
NC_000001.9:g.153530798A>C NCBI36
NG_011677.1:g.12052T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342741.6:c.968T>G MANE Select ENSP00000339933.4:p.Phe323Cys
ENST00000342741.4:c.968T>G ENSP00000339933.4:p.Phe323Cys
ENST00000392414.7:c.875T>G ENSP00000376214.3:p.Phe292Cys
NM_000298.5:c.968T>G NP_000289.1:p.Phe323Cys
NM_181871.3:c.875T>G NP_870986.1:p.Phe292Cys
XM_005245266.3:c.1127T>G XP_005245323.1:p.Phe376Cys
XM_006711386.2:c.776T>G XP_006711449.1:p.Phe259Cys
XM_011509639.1:c.1127T>G XP_011507941.1:p.Phe376Cys
XM_011509640.1:c.776T>G XP_011507942.1:p.Phe259Cys
NM_000298.6:c.968T>G MANE Select NP_000289.1:p.Phe323Cys
XM_006711386.4:c.776T>G XP_006711449.1:p.Phe259Cys
XM_011509640.3:c.776T>G XP_011507942.1:p.Phe259Cys
XM_017001493.1:c.968T>G XP_016856982.1:p.Phe323Cys
NM_181871.4:c.875T>G NP_870986.1:p.Phe292Cys