Canonical Allele Identifier: CA368020210

Gene: PCLO

Linked Data

• MyVariant Identifiers: chr7:g.82453626T>G (hg19) ; chr7:g.82824310T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824310T>G , CM000669.2:g.82824310T>G	GRCh38
NC_000007.13:g.82453626T>G , CM000669.1:g.82453626T>G	GRCh37
NC_000007.12:g.82291562T>G	NCBI36
NG_047145.1:g.343572A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000333891.14:c.14522A>C MANE Select	ENSP00000334319.8:p.Gln4841Pro
ENST00000333891.13:c.14522A>C	ENSP00000334319.8:p.Gln4841Pro
ENST00000423517.6:c.14522A>C	ENSP00000388393.2:p.Gln4841Pro
ENST00000426442.6:n.1017A>C
ENST00000618073.1:c.785A>C	ENSP00000482390.1:p.Gln262Pro
NM_014510.2:c.14522A>C	NP_055325.2:p.Gln4841Pro
NM_033026.5:c.14522A>C	NP_149015.2:p.Gln4841Pro
XM_017012006.2:c.7427A>C	XP_016867495.1:p.Gln2476Pro
XM_017012007.1:c.7400A>C	XP_016867496.1:p.Gln2467Pro
XR_001744643.2:n.16091A>C
NM_033026.6:c.14522A>C MANE Select	NP_149015.2:p.Gln4841Pro
NM_014510.3:c.14522A>C	NP_055325.2:p.Gln4841Pro