Canonical Allele Identifier: CA2683548856

Gene: PCLO

Linked Data

• gnomAD v4: 7-82824215-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824216_82824217del , CM000669.2:g.82824216_82824217del	GRCh38
NC_000007.13:g.82453532_82453533del , CM000669.1:g.82453532_82453533del	GRCh37
NC_000007.12:g.82291468_82291469del	NCBI36
NG_047145.1:g.343665_343666del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333891.14:c.14596+19_14596+20del MANE Select	ENSP00000334319.8:n.14596+19_14596+20del
ENST00000333891.13:c.14596+19_14596+20del	ENSP00000334319.8:n.14596+19_14596+20del
ENST00000423517.6:c.14596+19_14596+20del	ENSP00000388393.2:n.14596+19_14596+20del
ENST00000426442.6:n.1091+19_1091+20del
ENST00000618073.1:c.859+19_859+20del	ENSP00000482390.1:n.859+19_859+20del
NM_014510.2:c.14596+19_14596+20del	NP_055325.2:n.14596+19_14596+20del
NM_033026.5:c.14596+19_14596+20del	NP_149015.2:n.14596+19_14596+20del
XM_017012006.2:c.7501+19_7501+20del	XP_016867495.1:n.7501+19_7501+20del
XM_017012007.1:c.7474+19_7474+20del	XP_016867496.1:n.7474+19_7474+20del
XR_001744643.2:n.16165+19_16165+20del
NM_033026.6:c.14596+19_14596+20del MANE Select	NP_149015.2:n.14596+19_14596+20del
NM_014510.3:c.14596+19_14596+20del	NP_055325.2:n.14596+19_14596+20del