Canonical Allele Identifier: CA4319601
Gene: PCLO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.82916814C>T , CM000669.2:g.82916814C>T GRCh38
NC_000007.13:g.82546130C>T , CM000669.1:g.82546130C>T GRCh37
NC_000007.12:g.82384066C>T NCBI36
NG_047145.1:g.251068G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333891.14:c.11172G>A MANE Select ENSP00000334319.8:p.Leu3724=
ENST00000333891.13:c.11172G>A ENSP00000334319.8:p.Leu3724=
ENST00000423517.6:c.11172G>A ENSP00000388393.2:p.Leu3724=
ENST00000437081.1:c.1332G>A ENSP00000393760.1:p.Leu444=
NM_014510.2:c.11172G>A NP_055325.2:p.Leu3724=
NM_033026.5:c.11172G>A NP_149015.2:p.Leu3724=
XM_017012006.2:c.4077G>A XP_016867495.1:p.Leu1359=
XM_017012007.1:c.4077G>A XP_016867496.1:p.Leu1359=
XR_001744643.2:n.12741G>A
NM_033026.6:c.11172G>A MANE Select NP_149015.2:p.Leu3724=
NM_014510.3:c.11172G>A NP_055325.2:p.Leu3724=