Canonical Allele Identifier: CA368020152

Gene: PCLO

Linked Data

• MyVariant Identifiers: chr7:g.82453615G>C (hg19) ; chr7:g.82824299G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824299G>C , CM000669.2:g.82824299G>C	GRCh38
NC_000007.13:g.82453615G>C , CM000669.1:g.82453615G>C	GRCh37
NC_000007.12:g.82291551G>C	NCBI36
NG_047145.1:g.343583C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000333891.14:c.14533C>G MANE Select	ENSP00000334319.8:p.Gln4845Glu
ENST00000333891.13:c.14533C>G	ENSP00000334319.8:p.Gln4845Glu
ENST00000423517.6:c.14533C>G	ENSP00000388393.2:p.Gln4845Glu
ENST00000426442.6:n.1028C>G
ENST00000618073.1:c.796C>G	ENSP00000482390.1:p.Gln266Glu
NM_014510.2:c.14533C>G	NP_055325.2:p.Gln4845Glu
NM_033026.5:c.14533C>G	NP_149015.2:p.Gln4845Glu
XM_017012006.2:c.7438C>G	XP_016867495.1:p.Gln2480Glu
XM_017012007.1:c.7411C>G	XP_016867496.1:p.Gln2471Glu
XR_001744643.2:n.16102C>G
NM_033026.6:c.14533C>G MANE Select	NP_149015.2:p.Gln4845Glu
NM_014510.3:c.14533C>G	NP_055325.2:p.Gln4845Glu