Canonical Allele Identifier: CA456286598

Gene: PCLO

Linked Data

• MyVariant Identifiers: chr7:g.82453631G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824315G>C , CM000669.2:g.82824315G>C	GRCh38
NC_000007.13:g.82453631G>C , CM000669.1:g.82453631G>C	GRCh37
NC_000007.12:g.82291567G>C	NCBI36
NG_047145.1:g.343567C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333891.14:c.14517C>G MANE Select	ENSP00000334319.8:p.Ser4839=
ENST00000333891.13:c.14517C>G	ENSP00000334319.8:p.Ser4839=
ENST00000423517.6:c.14517C>G	ENSP00000388393.2:p.Ser4839=
ENST00000426442.6:n.1012C>G
ENST00000618073.1:c.780C>G	ENSP00000482390.1:p.Ser260=
NM_014510.2:c.14517C>G	NP_055325.2:p.Ser4839=
NM_033026.5:c.14517C>G	NP_149015.2:p.Ser4839=
XM_017012006.2:c.7422C>G	XP_016867495.1:p.Ser2474=
XM_017012007.1:c.7395C>G	XP_016867496.1:p.Ser2465=
XR_001744643.2:n.16086C>G
NM_033026.6:c.14517C>G MANE Select	NP_149015.2:p.Ser4839=
NM_014510.3:c.14517C>G	NP_055325.2:p.Ser4839=