Canonical Allele Identifier: CA2839099532
Gene: PKLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155290537C>A , CM000663.2:g.155290537C>A GRCh38
NC_000001.10:g.155260328C>A , CM000663.1:g.155260328C>A GRCh37
NC_000001.9:g.153526952C>A NCBI36
NG_011677.1:g.15898G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342741.6:c.*35G>T MANE Select ENSP00000339933.4:n.*35G>T
ENST00000342741.4:c.*35G>T ENSP00000339933.4:n.*35G>T
ENST00000392414.7:c.*35G>T ENSP00000376214.3:n.*35G>T
NM_000298.5:c.*35G>T NP_000289.1:n.*35G>T
NM_181871.3:c.*35G>T NP_870986.1:n.*35G>T
XM_005245266.3:c.*35G>T XP_005245323.1:n.*35G>T
XM_006711386.2:c.*35G>T XP_006711449.1:n.*35G>T
XM_011509640.1:c.*35G>T XP_011507942.1:n.*35G>T
NM_000298.6:c.*35G>T MANE Select NP_000289.1:n.*35G>T
XM_006711386.4:c.*35G>T XP_006711449.1:n.*35G>T
XM_011509640.3:c.*35G>T XP_011507942.1:n.*35G>T
NM_181871.4:c.*35G>T NP_870986.1:n.*35G>T