Canonical Allele Identifier: CA1721404352
Gene: PCLO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.82824313C= , CM000669.2:g.82824313C= GRCh38
NC_000007.13:g.82453629C= , CM000669.1:g.82453629C= GRCh37
NC_000007.12:g.82291565C= NCBI36
NG_047145.1:g.343569G=

Transcript Alleles

HGVS Amino-acid change
ENST00000333891.14:c.14519G= MANE Select ENSP00000334319.8:p.Ser4840=
ENST00000333891.13:c.14519G= ENSP00000334319.8:p.Ser4840=
ENST00000423517.6:c.14519G= ENSP00000388393.2:p.Ser4840=
ENST00000426442.6:n.1014G=
ENST00000618073.1:c.782G= ENSP00000482390.1:p.Ser261=
NM_014510.2:c.14519G= NP_055325.2:p.Ser4840=
NM_033026.5:c.14519G= NP_149015.2:p.Ser4840=
XM_017012006.2:c.7424G= XP_016867495.1:p.Ser2475=
XM_017012007.1:c.7397G= XP_016867496.1:p.Ser2466=
XR_001744643.2:n.16088G=
NM_033026.6:c.14519G= MANE Select NP_149015.2:p.Ser4840=
NM_014510.3:c.14519G= NP_055325.2:p.Ser4840=