Canonical Allele Identifier: CA368020536

Gene: PCLO

Linked Data

• gnomAD v4: 7-82824400-G-T
• MyVariant Identifiers: chr7:g.82453716G>T (hg19) ; chr7:g.82824400G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824400G>T , CM000669.2:g.82824400G>T	GRCh38
NC_000007.13:g.82453716G>T , CM000669.1:g.82453716G>T	GRCh37
NC_000007.12:g.82291652G>T	NCBI36
NG_047145.1:g.343482C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000333891.14:c.14432C>A MANE Select	ENSP00000334319.8:p.Ser4811Tyr
ENST00000333891.13:c.14432C>A	ENSP00000334319.8:p.Ser4811Tyr
ENST00000423517.6:c.14432C>A	ENSP00000388393.2:p.Ser4811Tyr
ENST00000426442.6:n.927C>A
ENST00000618073.1:c.695C>A	ENSP00000482390.1:p.Ser232Tyr
NM_014510.2:c.14432C>A	NP_055325.2:p.Ser4811Tyr
NM_033026.5:c.14432C>A	NP_149015.2:p.Ser4811Tyr
XM_017012006.2:c.7337C>A	XP_016867495.1:p.Ser2446Tyr
XM_017012007.1:c.7310C>A	XP_016867496.1:p.Ser2437Tyr
XR_001744643.2:n.16001C>A
NM_033026.6:c.14432C>A MANE Select	NP_149015.2:p.Ser4811Tyr
NM_014510.3:c.14432C>A	NP_055325.2:p.Ser4811Tyr