Canonical Allele Identifier: CA1721404387
Gene: PCLO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.82824392A= , CM000669.2:g.82824392A= GRCh38
NC_000007.13:g.82453708A= , CM000669.1:g.82453708A= GRCh37
NC_000007.12:g.82291644A= NCBI36
NG_047145.1:g.343490T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333891.14:c.14440T= MANE Select ENSP00000334319.8:p.Ser4814=
ENST00000333891.13:c.14440T= ENSP00000334319.8:p.Ser4814=
ENST00000423517.6:c.14440T= ENSP00000388393.2:p.Ser4814=
ENST00000426442.6:n.935T=
ENST00000618073.1:c.703T= ENSP00000482390.1:p.Ser235=
NM_014510.2:c.14440T= NP_055325.2:p.Ser4814=
NM_033026.5:c.14440T= NP_149015.2:p.Ser4814=
XM_017012006.2:c.7345T= XP_016867495.1:p.Ser2449=
XM_017012007.1:c.7318T= XP_016867496.1:p.Ser2440=
XR_001744643.2:n.16009T=
NM_033026.6:c.14440T= MANE Select NP_149015.2:p.Ser4814=
NM_014510.3:c.14440T= NP_055325.2:p.Ser4814=