Canonical Allele Identifier: CA1721404390
Gene: PCLO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.82824396G= , CM000669.2:g.82824396G= GRCh38
NC_000007.13:g.82453712G= , CM000669.1:g.82453712G= GRCh37
NC_000007.12:g.82291648G= NCBI36
NG_047145.1:g.343486C=

Transcript Alleles

HGVS Amino-acid change
ENST00000333891.14:c.14436C= MANE Select ENSP00000334319.8:p.Ser4812=
ENST00000333891.13:c.14436C= ENSP00000334319.8:p.Ser4812=
ENST00000423517.6:c.14436C= ENSP00000388393.2:p.Ser4812=
ENST00000426442.6:n.931C=
ENST00000618073.1:c.699C= ENSP00000482390.1:p.Ser233=
NM_014510.2:c.14436C= NP_055325.2:p.Ser4812=
NM_033026.5:c.14436C= NP_149015.2:p.Ser4812=
XM_017012006.2:c.7341C= XP_016867495.1:p.Ser2447=
XM_017012007.1:c.7314C= XP_016867496.1:p.Ser2438=
XR_001744643.2:n.16005C=
NM_033026.6:c.14436C= MANE Select NP_149015.2:p.Ser4812=
NM_014510.3:c.14436C= NP_055325.2:p.Ser4812=