Canonical Allele Identifier: CA1721402816
Gene: PCLO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.82820719A= , CM000669.2:g.82820719A= GRCh38
NC_000007.13:g.82450035A= , CM000669.1:g.82450035A= GRCh37
NC_000007.12:g.82287971A= NCBI36
NG_047145.1:g.347163T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333891.14:c.14791+1776T= MANE Select ENSP00000334319.8:n.14791+1776T=
ENST00000333891.13:c.14791+1776T= ENSP00000334319.8:n.14791+1776T=
ENST00000423517.6:c.*1759T= ENSP00000388393.2:n.*1759T=
ENST00000432078.2:n.279+393T=
NM_014510.2:c.*1759T= NP_055325.2:n.*1759T=
NM_033026.5:c.14791+1776T= NP_149015.2:n.14791+1776T=
XM_017012006.2:c.7879+393T= XP_016867495.1:n.7879+393T=
XR_001744643.2:n.17743+393T=
NM_033026.6:c.14791+1776T= MANE Select NP_149015.2:n.14791+1776T=
NM_014510.3:c.*1759T= NP_055325.2:n.*1759T=