Canonical Allele Identifier: CA456286643
Gene: PCLO HGNC NCBI

Linked Data

gnomAD v4: 7-82824393-T-A
MyVariant Identifiers: chr7:g.82453709T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.82824393T>A , CM000669.2:g.82824393T>A GRCh38
NC_000007.13:g.82453709T>A , CM000669.1:g.82453709T>A GRCh37
NC_000007.12:g.82291645T>A NCBI36
NG_047145.1:g.343489A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333891.14:c.14439A>T MANE Select ENSP00000334319.8:p.Thr4813=
ENST00000333891.13:c.14439A>T ENSP00000334319.8:p.Thr4813=
ENST00000423517.6:c.14439A>T ENSP00000388393.2:p.Thr4813=
ENST00000426442.6:n.934A>T
ENST00000618073.1:c.702A>T ENSP00000482390.1:p.Thr234=
NM_014510.2:c.14439A>T NP_055325.2:p.Thr4813=
NM_033026.5:c.14439A>T NP_149015.2:p.Thr4813=
XM_017012006.2:c.7344A>T XP_016867495.1:p.Thr2448=
XM_017012007.1:c.7317A>T XP_016867496.1:p.Thr2439=
XR_001744643.2:n.16008A>T
NM_033026.6:c.14439A>T MANE Select NP_149015.2:p.Thr4813=
NM_014510.3:c.14439A>T NP_055325.2:p.Thr4813=