Canonical Allele Identifier: CA368020549

Gene: PCLO

Linked Data

• dbSNP Id: rs1791881509
• gnomAD v4: 7-82824406-T-A
• MyVariant Identifiers: chr7:g.82453722T>A (hg19) ; chr7:g.82824406T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824406T>A , CM000669.2:g.82824406T>A	GRCh38
NC_000007.13:g.82453722T>A , CM000669.1:g.82453722T>A	GRCh37
NC_000007.12:g.82291658T>A	NCBI36
NG_047145.1:g.343476A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000333891.14:c.14426A>T MANE Select	ENSP00000334319.8:p.Asp4809Val
ENST00000333891.13:c.14426A>T	ENSP00000334319.8:p.Asp4809Val
ENST00000423517.6:c.14426A>T	ENSP00000388393.2:p.Asp4809Val
ENST00000426442.6:n.921A>T
ENST00000618073.1:c.689A>T	ENSP00000482390.1:p.Asp230Val
NM_014510.2:c.14426A>T	NP_055325.2:p.Asp4809Val
NM_033026.5:c.14426A>T	NP_149015.2:p.Asp4809Val
XM_017012006.2:c.7331A>T	XP_016867495.1:p.Asp2444Val
XM_017012007.1:c.7304A>T	XP_016867496.1:p.Asp2435Val
XR_001744643.2:n.15995A>T
NM_033026.6:c.14426A>T MANE Select	NP_149015.2:p.Asp4809Val
NM_014510.3:c.14426A>T	NP_055325.2:p.Asp4809Val