Canonical Allele Identifier: CA1721404343
Gene: PCLO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.82824296A= , CM000669.2:g.82824296A= GRCh38
NC_000007.13:g.82453612A= , CM000669.1:g.82453612A= GRCh37
NC_000007.12:g.82291548A= NCBI36
NG_047145.1:g.343586T=

Transcript Alleles

HGVS Amino-acid change
ENST00000333891.14:c.14536T= MANE Select ENSP00000334319.8:p.Ser4846=
ENST00000333891.13:c.14536T= ENSP00000334319.8:p.Ser4846=
ENST00000423517.6:c.14536T= ENSP00000388393.2:p.Ser4846=
ENST00000426442.6:n.1031T=
ENST00000618073.1:c.799T= ENSP00000482390.1:p.Ser267=
NM_014510.2:c.14536T= NP_055325.2:p.Ser4846=
NM_033026.5:c.14536T= NP_149015.2:p.Ser4846=
XM_017012006.2:c.7441T= XP_016867495.1:p.Ser2481=
XM_017012007.1:c.7414T= XP_016867496.1:p.Ser2472=
XR_001744643.2:n.16105T=
NM_033026.6:c.14536T= MANE Select NP_149015.2:p.Ser4846=
NM_014510.3:c.14536T= NP_055325.2:p.Ser4846=