Canonical Allele Identifier: CA1721404294
Gene: PCLO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.82824197A= , CM000669.2:g.82824197A= GRCh38
NC_000007.13:g.82453513A= , CM000669.1:g.82453513A= GRCh37
NC_000007.12:g.82291449A= NCBI36
NG_047145.1:g.343685T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333891.14:c.14596+39T= MANE Select ENSP00000334319.8:n.14596+39T=
ENST00000333891.13:c.14596+39T= ENSP00000334319.8:n.14596+39T=
ENST00000423517.6:c.14596+39T= ENSP00000388393.2:n.14596+39T=
ENST00000426442.6:n.1091+39T=
ENST00000618073.1:c.859+39T= ENSP00000482390.1:n.859+39T=
NM_014510.2:c.14596+39T= NP_055325.2:n.14596+39T=
NM_033026.5:c.14596+39T= NP_149015.2:n.14596+39T=
XM_017012006.2:c.7501+39T= XP_016867495.1:n.7501+39T=
XM_017012007.1:c.7474+39T= XP_016867496.1:n.7474+39T=
XR_001744643.2:n.16165+39T=
NM_033026.6:c.14596+39T= MANE Select NP_149015.2:n.14596+39T=
NM_014510.3:c.14596+39T= NP_055325.2:n.14596+39T=