Canonical Allele Identifier: CA1721404395
Gene: PCLO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.82824403A= , CM000669.2:g.82824403A= GRCh38
NC_000007.13:g.82453719A= , CM000669.1:g.82453719A= GRCh37
NC_000007.12:g.82291655A= NCBI36
NG_047145.1:g.343479T=

Transcript Alleles

HGVS Amino-acid change
ENST00000333891.14:c.14429T= MANE Select ENSP00000334319.8:p.Leu4810=
ENST00000333891.13:c.14429T= ENSP00000334319.8:p.Leu4810=
ENST00000423517.6:c.14429T= ENSP00000388393.2:p.Leu4810=
ENST00000426442.6:n.924T=
ENST00000618073.1:c.692T= ENSP00000482390.1:p.Leu231=
NM_014510.2:c.14429T= NP_055325.2:p.Leu4810=
NM_033026.5:c.14429T= NP_149015.2:p.Leu4810=
XM_017012006.2:c.7334T= XP_016867495.1:p.Leu2445=
XM_017012007.1:c.7307T= XP_016867496.1:p.Leu2436=
XR_001744643.2:n.15998T=
NM_033026.6:c.14429T= MANE Select NP_149015.2:p.Leu4810=
NM_014510.3:c.14429T= NP_055325.2:p.Leu4810=