Canonical Allele Identifier: CA576268395

Gene: PCLO

Linked Data

• dbSNP Id: rs1562802405
• gnomAD v2: 7-82453531-AC-A
• MyVariant Identifiers: chr7:g.82453532del (hg19) ; chr7:g.82824216del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824216del , CM000669.2:g.82824216del	GRCh38
NC_000007.13:g.82453532del , CM000669.1:g.82453532del	GRCh37
NC_000007.12:g.82291468del	NCBI36
NG_047145.1:g.343666del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333891.14:c.14596+20del MANE Select	ENSP00000334319.8:n.14596+20del
ENST00000333891.13:c.14596+20del	ENSP00000334319.8:n.14596+20del
ENST00000423517.6:c.14596+20del	ENSP00000388393.2:n.14596+20del
ENST00000426442.6:n.1091+20del
ENST00000618073.1:c.859+20del	ENSP00000482390.1:n.859+20del
NM_014510.2:c.14596+20del	NP_055325.2:n.14596+20del
NM_033026.5:c.14596+20del	NP_149015.2:n.14596+20del
XM_017012006.2:c.7501+20del	XP_016867495.1:n.7501+20del
XM_017012007.1:c.7474+20del	XP_016867496.1:n.7474+20del
XR_001744643.2:n.16165+20del
NM_033026.6:c.14596+20del MANE Select	NP_149015.2:n.14596+20del
NM_014510.3:c.14596+20del	NP_055325.2:n.14596+20del