Canonical Allele Identifier: CA368020548

Gene: PCLO

Linked Data

• MyVariant Identifiers: chr7:g.82453721A>T (hg19) ; chr7:g.82824405A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824405A>T , CM000669.2:g.82824405A>T	GRCh38
NC_000007.13:g.82453721A>T , CM000669.1:g.82453721A>T	GRCh37
NC_000007.12:g.82291657A>T	NCBI36
NG_047145.1:g.343477T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333891.14:c.14427T>A MANE Select	ENSP00000334319.8:p.Asp4809Glu
ENST00000333891.13:c.14427T>A	ENSP00000334319.8:p.Asp4809Glu
ENST00000423517.6:c.14427T>A	ENSP00000388393.2:p.Asp4809Glu
ENST00000426442.6:n.922T>A
ENST00000618073.1:c.690T>A	ENSP00000482390.1:p.Asp230Glu
NM_014510.2:c.14427T>A	NP_055325.2:p.Asp4809Glu
NM_033026.5:c.14427T>A	NP_149015.2:p.Asp4809Glu
XM_017012006.2:c.7332T>A	XP_016867495.1:p.Asp2444Glu
XM_017012007.1:c.7305T>A	XP_016867496.1:p.Asp2435Glu
XR_001744643.2:n.15996T>A
NM_033026.6:c.14427T>A MANE Select	NP_149015.2:p.Asp4809Glu
NM_014510.3:c.14427T>A	NP_055325.2:p.Asp4809Glu