Canonical Allele Identifier: CA1144210
Gene: PKLR HGNC NCBI

Linked Data

dbSNP Id: rs764143249

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155294648G>T , CM000663.2:g.155294648G>T GRCh38
NC_000001.10:g.155264439G>T , CM000663.1:g.155264439G>T GRCh37
NC_000001.9:g.153531063G>T NCBI36
NG_011677.1:g.11787C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000342741.6:c.799C>A MANE Select ENSP00000339933.4:p.Gln267Lys
ENST00000342741.4:c.799C>A ENSP00000339933.4:p.Gln267Lys
ENST00000392414.7:c.706C>A ENSP00000376214.3:p.Gln236Lys
NM_000298.5:c.799C>A NP_000289.1:p.Gln267Lys
NM_181871.3:c.706C>A NP_870986.1:p.Gln236Lys
XM_005245266.3:c.958C>A XP_005245323.1:p.Gln320Lys
XM_006711386.2:c.607C>A XP_006711449.1:p.Gln203Lys
XM_011509639.1:c.958C>A XP_011507941.1:p.Gln320Lys
XM_011509640.1:c.607C>A XP_011507942.1:p.Gln203Lys
NM_000298.6:c.799C>A MANE Select NP_000289.1:p.Gln267Lys
XM_006711386.4:c.607C>A XP_006711449.1:p.Gln203Lys
XM_011509640.3:c.607C>A XP_011507942.1:p.Gln203Lys
XM_017001493.1:c.799C>A XP_016856982.1:p.Gln267Lys
NM_181871.4:c.706C>A NP_870986.1:p.Gln236Lys