Canonical Allele Identifier: CA1721402817
Gene: PCLO HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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