Canonical Allele Identifier: CA368020234

Gene: PCLO

Linked Data

• COSMIC: COSM3640950 ; COSM3640951 ; COSM4899166
• MyVariant Identifiers: chr7:g.82453632G>A (hg19) ; chr7:g.82824316G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824316G>A , CM000669.2:g.82824316G>A	GRCh38
NC_000007.13:g.82453632G>A , CM000669.1:g.82453632G>A	GRCh37
NC_000007.12:g.82291568G>A	NCBI36
NG_047145.1:g.343566C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333891.14:c.14516C>T MANE Select	ENSP00000334319.8:p.Ser4839Phe
ENST00000333891.13:c.14516C>T	ENSP00000334319.8:p.Ser4839Phe
ENST00000423517.6:c.14516C>T	ENSP00000388393.2:p.Ser4839Phe
ENST00000426442.6:n.1011C>T
ENST00000618073.1:c.779C>T	ENSP00000482390.1:p.Ser260Phe
NM_014510.2:c.14516C>T	NP_055325.2:p.Ser4839Phe
NM_033026.5:c.14516C>T	NP_149015.2:p.Ser4839Phe
XM_017012006.2:c.7421C>T	XP_016867495.1:p.Ser2474Phe
XM_017012007.1:c.7394C>T	XP_016867496.1:p.Ser2465Phe
XR_001744643.2:n.16085C>T
NM_033026.6:c.14516C>T MANE Select	NP_149015.2:p.Ser4839Phe
NM_014510.3:c.14516C>T	NP_055325.2:p.Ser4839Phe