Canonical Allele Identifier: CA1721404351
Gene: PCLO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.82824311G= , CM000669.2:g.82824311G= GRCh38
NC_000007.13:g.82453627G= , CM000669.1:g.82453627G= GRCh37
NC_000007.12:g.82291563G= NCBI36
NG_047145.1:g.343571C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333891.14:c.14521C= MANE Select ENSP00000334319.8:p.Gln4841=
ENST00000333891.13:c.14521C= ENSP00000334319.8:p.Gln4841=
ENST00000423517.6:c.14521C= ENSP00000388393.2:p.Gln4841=
ENST00000426442.6:n.1016C=
ENST00000618073.1:c.784C= ENSP00000482390.1:p.Gln262=
NM_014510.2:c.14521C= NP_055325.2:p.Gln4841=
NM_033026.5:c.14521C= NP_149015.2:p.Gln4841=
XM_017012006.2:c.7426C= XP_016867495.1:p.Gln2476=
XM_017012007.1:c.7399C= XP_016867496.1:p.Gln2467=
XR_001744643.2:n.16090C=
NM_033026.6:c.14521C= MANE Select NP_149015.2:p.Gln4841=
NM_014510.3:c.14521C= NP_055325.2:p.Gln4841=