Canonical Allele Identifier: CA456286641

Gene: PCLO

Linked Data

• dbSNP Id: rs1216904779
• MyVariant Identifiers: chr7:g.82453709T>G (hg19) ; chr7:g.82824393T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824393T>G , CM000669.2:g.82824393T>G	GRCh38
NC_000007.13:g.82453709T>G , CM000669.1:g.82453709T>G	GRCh37
NC_000007.12:g.82291645T>G	NCBI36
NG_047145.1:g.343489A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000333891.14:c.14439A>C MANE Select	ENSP00000334319.8:p.Thr4813=
ENST00000333891.13:c.14439A>C	ENSP00000334319.8:p.Thr4813=
ENST00000423517.6:c.14439A>C	ENSP00000388393.2:p.Thr4813=
ENST00000426442.6:n.934A>C
ENST00000618073.1:c.702A>C	ENSP00000482390.1:p.Thr234=
NM_014510.2:c.14439A>C	NP_055325.2:p.Thr4813=
NM_033026.5:c.14439A>C	NP_149015.2:p.Thr4813=
XM_017012006.2:c.7344A>C	XP_016867495.1:p.Thr2448=
XM_017012007.1:c.7317A>C	XP_016867496.1:p.Thr2439=
XR_001744643.2:n.16008A>C
NM_033026.6:c.14439A>C MANE Select	NP_149015.2:p.Thr4813=
NM_014510.3:c.14439A>C	NP_055325.2:p.Thr4813=