Canonical Allele Identifier: CA2481225419
Gene: PKLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155291860T= , CM000663.2:g.155291860T= GRCh38
NC_000001.10:g.155261651T= , CM000663.1:g.155261651T= GRCh37
NC_000001.9:g.153528275T= NCBI36
NG_011677.1:g.14575A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342741.6:c.1514A= MANE Select ENSP00000339933.4:p.Gln505=
ENST00000342741.4:c.1514A= ENSP00000339933.4:p.Gln505=
ENST00000392414.7:c.1421A= ENSP00000376214.3:p.Gln474=
NM_000298.5:c.1514A= NP_000289.1:p.Gln505=
NM_181871.3:c.1421A= NP_870986.1:p.Gln474=
XM_005245266.3:c.1673A= XP_005245323.1:p.Gln558=
XM_006711386.2:c.1322A= XP_006711449.1:p.Gln441=
XM_011509640.1:c.1322A= XP_011507942.1:p.Gln441=
NM_000298.6:c.1514A= MANE Select NP_000289.1:p.Gln505=
XM_006711386.4:c.1322A= XP_006711449.1:p.Gln441=
XM_011509640.3:c.1322A= XP_011507942.1:p.Gln441=
NM_181871.4:c.1421A= NP_870986.1:p.Gln474=