Canonical Allele Identifier: CA2838499501
Gene: PKLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155290529A>G , CM000663.2:g.155290529A>G GRCh38
NC_000001.10:g.155260320A>G , CM000663.1:g.155260320A>G GRCh37
NC_000001.9:g.153526944A>G NCBI36
NG_011677.1:g.15906T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342741.6:c.*43T>C MANE Select ENSP00000339933.4:n.*43T>C
ENST00000342741.4:c.*43T>C ENSP00000339933.4:n.*43T>C
ENST00000392414.7:c.*43T>C ENSP00000376214.3:n.*43T>C
NM_000298.5:c.*43T>C NP_000289.1:n.*43T>C
NM_181871.3:c.*43T>C NP_870986.1:n.*43T>C
XM_005245266.3:c.*43T>C XP_005245323.1:n.*43T>C
XM_006711386.2:c.*43T>C XP_006711449.1:n.*43T>C
XM_011509640.1:c.*43T>C XP_011507942.1:n.*43T>C
NM_000298.6:c.*43T>C MANE Select NP_000289.1:n.*43T>C
XM_006711386.4:c.*43T>C XP_006711449.1:n.*43T>C
XM_011509640.3:c.*43T>C XP_011507942.1:n.*43T>C
NM_181871.4:c.*43T>C NP_870986.1:n.*43T>C