Canonical Allele Identifier: CA1721404348
Gene: PCLO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.82824303G= , CM000669.2:g.82824303G= GRCh38
NC_000007.13:g.82453619G= , CM000669.1:g.82453619G= GRCh37
NC_000007.12:g.82291555G= NCBI36
NG_047145.1:g.343579C=

Transcript Alleles

HGVS Amino-acid change
ENST00000333891.14:c.14529C= MANE Select ENSP00000334319.8:p.Ser4843=
ENST00000333891.13:c.14529C= ENSP00000334319.8:p.Ser4843=
ENST00000423517.6:c.14529C= ENSP00000388393.2:p.Ser4843=
ENST00000426442.6:n.1024C=
ENST00000618073.1:c.792C= ENSP00000482390.1:p.Ser264=
NM_014510.2:c.14529C= NP_055325.2:p.Ser4843=
NM_033026.5:c.14529C= NP_149015.2:p.Ser4843=
XM_017012006.2:c.7434C= XP_016867495.1:p.Ser2478=
XM_017012007.1:c.7407C= XP_016867496.1:p.Ser2469=
XR_001744643.2:n.16098C=
NM_033026.6:c.14529C= MANE Select NP_149015.2:p.Ser4843=
NM_014510.3:c.14529C= NP_055325.2:p.Ser4843=