Canonical Allele Identifier: CA2739266505

Gene: PCLO

Linked Data

• ClinVar Variation Id: 2846352
• ClinVar RCV Id: RCV003687847

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824218dup , CM000669.2:g.82824218dup	GRCh38
NC_000007.13:g.82453534dup , CM000669.1:g.82453534dup	GRCh37
NC_000007.12:g.82291470dup	NCBI36
NG_047145.1:g.343665dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333891.14:c.14596+19dup MANE Select	ENSP00000334319.8:n.14596+19dup
ENST00000333891.13:c.14596+19dup	ENSP00000334319.8:n.14596+19dup
ENST00000423517.6:c.14596+19dup	ENSP00000388393.2:n.14596+19dup
ENST00000426442.6:n.1091+19dup
ENST00000618073.1:c.859+19dup	ENSP00000482390.1:n.859+19dup
NM_014510.2:c.14596+19dup	NP_055325.2:n.14596+19dup
NM_033026.5:c.14596+19dup	NP_149015.2:n.14596+19dup
XM_017012006.2:c.7501+19dup	XP_016867495.1:n.7501+19dup
XM_017012007.1:c.7474+19dup	XP_016867496.1:n.7474+19dup
XR_001744643.2:n.16165+19dup
NM_033026.6:c.14596+19dup MANE Select	NP_149015.2:n.14596+19dup
NM_014510.3:c.14596+19dup	NP_055325.2:n.14596+19dup