Canonical Allele Identifier: CA4320799
Gene: PCLO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.82956358C>T , CM000669.2:g.82956358C>T GRCh38
NC_000007.13:g.82585674C>T , CM000669.1:g.82585674C>T GRCh37
NC_000007.12:g.82423610C>T NCBI36
NG_047145.1:g.211524G>A

Transcript Alleles

HGVS Amino-acid Change
NM_033026.6:c.4595G>A MANE Select NP_149015.2:p.Ser1532Asn
ENST00000333891.14:c.4595G>A MANE Select ENSP00000334319.8:p.Ser1532Asn
NM_014510.2:c.4595G>A NP_055325.2:p.Ser1532Asn
NM_014510.3:c.4595G>A NP_055325.2:p.Ser1532Asn
NM_033026.5:c.4595G>A NP_149015.2:p.Ser1532Asn
ENST00000333891.13:c.4595G>A ENSP00000334319.8:p.Ser1532Asn
ENST00000423517.6:c.4595G>A ENSP00000388393.2:p.Ser1532Asn
XM_017012006.2:c.4017+9413G>A XP_016867495.1:n.4017+9413G>A
XM_017012007.1:c.4017+9413G>A XP_016867496.1:n.4017+9413G>A
XR_001744643.2:n.6164G>A