Canonical Allele Identifier: CA368020192

Gene: PCLO

Linked Data

• MyVariant Identifiers: chr7:g.82453623C>G (hg19) ; chr7:g.82824307C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824307C>G , CM000669.2:g.82824307C>G	GRCh38
NC_000007.13:g.82453623C>G , CM000669.1:g.82453623C>G	GRCh37
NC_000007.12:g.82291559C>G	NCBI36
NG_047145.1:g.343575G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333891.14:c.14525G>C MANE Select	ENSP00000334319.8:p.Ser4842Thr
ENST00000333891.13:c.14525G>C	ENSP00000334319.8:p.Ser4842Thr
ENST00000423517.6:c.14525G>C	ENSP00000388393.2:p.Ser4842Thr
ENST00000426442.6:n.1020G>C
ENST00000618073.1:c.788G>C	ENSP00000482390.1:p.Ser263Thr
NM_014510.2:c.14525G>C	NP_055325.2:p.Ser4842Thr
NM_033026.5:c.14525G>C	NP_149015.2:p.Ser4842Thr
XM_017012006.2:c.7430G>C	XP_016867495.1:p.Ser2477Thr
XM_017012007.1:c.7403G>C	XP_016867496.1:p.Ser2468Thr
XR_001744643.2:n.16094G>C
NM_033026.6:c.14525G>C MANE Select	NP_149015.2:p.Ser4842Thr
NM_014510.3:c.14525G>C	NP_055325.2:p.Ser4842Thr