Canonical Allele Identifier: CA2841104293
Gene: PKLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155290746dup , CM000663.2:g.155290746dup GRCh38
NC_000001.10:g.155260537dup , CM000663.1:g.155260537dup GRCh37
NC_000001.9:g.153527161dup NCBI36
NG_011677.1:g.15691dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000342741.6:c.1619-66dup MANE Select ENSP00000339933.4:n.1619-66dup
ENST00000342741.4:c.1619-66dup ENSP00000339933.4:n.1619-66dup
ENST00000392414.7:c.1526-66dup ENSP00000376214.3:n.1526-66dup
NM_000298.5:c.1619-66dup NP_000289.1:n.1619-66dup
NM_181871.3:c.1526-66dup NP_870986.1:n.1526-66dup
XM_005245266.3:c.1778-66dup XP_005245323.1:n.1778-66dup
XM_006711386.2:c.1427-66dup XP_006711449.1:n.1427-66dup
XM_011509640.1:c.1427-66dup XP_011507942.1:n.1427-66dup
NM_000298.6:c.1619-66dup MANE Select NP_000289.1:n.1619-66dup
XM_006711386.4:c.1427-66dup XP_006711449.1:n.1427-66dup
XM_011509640.3:c.1427-66dup XP_011507942.1:n.1427-66dup
NM_181871.4:c.1526-66dup NP_870986.1:n.1526-66dup