Canonical Allele Identifier: CA368020232

Gene: PCLO

Linked Data

• MyVariant Identifiers: chr7:g.82453630T>A (hg19) ; chr7:g.82824314T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824314T>A , CM000669.2:g.82824314T>A	GRCh38
NC_000007.13:g.82453630T>A , CM000669.1:g.82453630T>A	GRCh37
NC_000007.12:g.82291566T>A	NCBI36
NG_047145.1:g.343568A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333891.14:c.14518A>T MANE Select	ENSP00000334319.8:p.Ser4840Cys
ENST00000333891.13:c.14518A>T	ENSP00000334319.8:p.Ser4840Cys
ENST00000423517.6:c.14518A>T	ENSP00000388393.2:p.Ser4840Cys
ENST00000426442.6:n.1013A>T
ENST00000618073.1:c.781A>T	ENSP00000482390.1:p.Ser261Cys
NM_014510.2:c.14518A>T	NP_055325.2:p.Ser4840Cys
NM_033026.5:c.14518A>T	NP_149015.2:p.Ser4840Cys
XM_017012006.2:c.7423A>T	XP_016867495.1:p.Ser2475Cys
XM_017012007.1:c.7396A>T	XP_016867496.1:p.Ser2466Cys
XR_001744643.2:n.16087A>T
NM_033026.6:c.14518A>T MANE Select	NP_149015.2:p.Ser4840Cys
NM_014510.3:c.14518A>T	NP_055325.2:p.Ser4840Cys