Canonical Allele Identifier: CA1721404349
Gene: PCLO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.82824306G= , CM000669.2:g.82824306G= GRCh38
NC_000007.13:g.82453622G= , CM000669.1:g.82453622G= GRCh37
NC_000007.12:g.82291558G= NCBI36
NG_047145.1:g.343576C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333891.14:c.14526C= MANE Select ENSP00000334319.8:p.Ser4842=
ENST00000333891.13:c.14526C= ENSP00000334319.8:p.Ser4842=
ENST00000423517.6:c.14526C= ENSP00000388393.2:p.Ser4842=
ENST00000426442.6:n.1021C=
ENST00000618073.1:c.789C= ENSP00000482390.1:p.Ser263=
NM_014510.2:c.14526C= NP_055325.2:p.Ser4842=
NM_033026.5:c.14526C= NP_149015.2:p.Ser4842=
XM_017012006.2:c.7431C= XP_016867495.1:p.Ser2477=
XM_017012007.1:c.7404C= XP_016867496.1:p.Ser2468=
XR_001744643.2:n.16095C=
NM_033026.6:c.14526C= MANE Select NP_149015.2:p.Ser4842=
NM_014510.3:c.14526C= NP_055325.2:p.Ser4842=