Canonical Allele Identifier: CA456286650

Gene: PCLO

Linked Data

• MyVariant Identifiers: chr7:g.82453724A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824408A>T , CM000669.2:g.82824408A>T	GRCh38
NC_000007.13:g.82453724A>T , CM000669.1:g.82453724A>T	GRCh37
NC_000007.12:g.82291660A>T	NCBI36
NG_047145.1:g.343474T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000333891.14:c.14424T>A MANE Select	ENSP00000334319.8:p.Ile4808=
ENST00000333891.13:c.14424T>A	ENSP00000334319.8:p.Ile4808=
ENST00000423517.6:c.14424T>A	ENSP00000388393.2:p.Ile4808=
ENST00000426442.6:n.919T>A
ENST00000618073.1:c.687T>A	ENSP00000482390.1:p.Ile229=
NM_014510.2:c.14424T>A	NP_055325.2:p.Ile4808=
NM_033026.5:c.14424T>A	NP_149015.2:p.Ile4808=
XM_017012006.2:c.7329T>A	XP_016867495.1:p.Ile2443=
XM_017012007.1:c.7302T>A	XP_016867496.1:p.Ile2434=
XR_001744643.2:n.15993T>A
NM_033026.6:c.14424T>A MANE Select	NP_149015.2:p.Ile4808=
NM_014510.3:c.14424T>A	NP_055325.2:p.Ile4808=