Canonical Allele Identifier: CA456286673
Community Standard Title: NM_033026.6(PCLO):c.14409T>G (p.Leu4803=)
Gene: PCLO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.82826595A>C , CM000669.2:g.82826595A>C GRCh38
NC_000007.13:g.82455911A>C , CM000669.1:g.82455911A>C GRCh37
NC_000007.12:g.82293847A>C NCBI36
NG_047145.1:g.341287T>G

Transcript Alleles

HGVS Amino-acid Change
NM_033026.6:c.14409T>G MANE Select NP_149015.2:p.Leu4803=
ENST00000333891.14:c.14409T>G MANE Select ENSP00000334319.8:p.Leu4803=
NM_014510.2:c.14409T>G NP_055325.2:p.Leu4803=
NM_014510.3:c.14409T>G NP_055325.2:p.Leu4803=
NM_033026.5:c.14409T>G NP_149015.2:p.Leu4803=
ENST00000333891.13:c.14409T>G ENSP00000334319.8:p.Leu4803=
ENST00000423517.6:c.14409T>G ENSP00000388393.2:p.Leu4803=
ENST00000426442.6:n.904T>G
ENST00000618073.1:c.672T>G ENSP00000482390.1:p.Leu224=
XM_017012006.2:c.7314T>G XP_016867495.1:p.Leu2438=
XM_017012007.1:c.7287T>G XP_016867496.1:p.Leu2429=
XR_001744643.2:n.15978T>G