Canonical Allele Identifier: CA456286594

Gene: PCLO

Linked Data

• MyVariant Identifiers: chr7:g.82453625C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824309C>T , CM000669.2:g.82824309C>T	GRCh38
NC_000007.13:g.82453625C>T , CM000669.1:g.82453625C>T	GRCh37
NC_000007.12:g.82291561C>T	NCBI36
NG_047145.1:g.343573G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333891.14:c.14523G>A MANE Select	ENSP00000334319.8:p.Gln4841=
ENST00000333891.13:c.14523G>A	ENSP00000334319.8:p.Gln4841=
ENST00000423517.6:c.14523G>A	ENSP00000388393.2:p.Gln4841=
ENST00000426442.6:n.1018G>A
ENST00000618073.1:c.786G>A	ENSP00000482390.1:p.Gln262=
NM_014510.2:c.14523G>A	NP_055325.2:p.Gln4841=
NM_033026.5:c.14523G>A	NP_149015.2:p.Gln4841=
XM_017012006.2:c.7428G>A	XP_016867495.1:p.Gln2476=
XM_017012007.1:c.7401G>A	XP_016867496.1:p.Gln2467=
XR_001744643.2:n.16092G>A
NM_033026.6:c.14523G>A MANE Select	NP_149015.2:p.Gln4841=
NM_014510.3:c.14523G>A	NP_055325.2:p.Gln4841=