Canonical Allele Identifier: CA1721404397
Gene: PCLO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.82824406T= , CM000669.2:g.82824406T= GRCh38
NC_000007.13:g.82453722T= , CM000669.1:g.82453722T= GRCh37
NC_000007.12:g.82291658T= NCBI36
NG_047145.1:g.343476A=

Transcript Alleles

HGVS Amino-acid change
ENST00000333891.14:c.14426A= MANE Select ENSP00000334319.8:p.Asp4809=
ENST00000333891.13:c.14426A= ENSP00000334319.8:p.Asp4809=
ENST00000423517.6:c.14426A= ENSP00000388393.2:p.Asp4809=
ENST00000426442.6:n.921A=
ENST00000618073.1:c.689A= ENSP00000482390.1:p.Asp230=
NM_014510.2:c.14426A= NP_055325.2:p.Asp4809=
NM_033026.5:c.14426A= NP_149015.2:p.Asp4809=
XM_017012006.2:c.7331A= XP_016867495.1:p.Asp2444=
XM_017012007.1:c.7304A= XP_016867496.1:p.Asp2435=
XR_001744643.2:n.15995A=
NM_033026.6:c.14426A= MANE Select NP_149015.2:p.Asp4809=
NM_014510.3:c.14426A= NP_055325.2:p.Asp4809=