Canonical Allele Identifier: CA1721404309

Gene: PCLO

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824215_82824216delinsAC , CM000669.2:g.82824215_82824216delinsAC	GRCh38
NC_000007.13:g.82453531_82453532delinsAC , CM000669.1:g.82453531_82453532delinsAC	GRCh37
NC_000007.12:g.82291467_82291468delinsAC	NCBI36
NG_047145.1:g.343666_343667delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333891.14:c.14596+20_14596+21delinsGT MANE Select	ENSP00000334319.8:n.14596+20_14596+21delinsGT
ENST00000333891.13:c.14596+20_14596+21delinsGT	ENSP00000334319.8:n.14596+20_14596+21delinsGT
ENST00000423517.6:c.14596+20_14596+21delinsGT	ENSP00000388393.2:n.14596+20_14596+21delinsGT
ENST00000426442.6:n.1091+20_1091+21delinsGT
ENST00000618073.1:c.859+20_859+21delinsGT	ENSP00000482390.1:n.859+20_859+21delinsGT
NM_014510.2:c.14596+20_14596+21delinsGT	NP_055325.2:n.14596+20_14596+21delinsGT
NM_033026.5:c.14596+20_14596+21delinsGT	NP_149015.2:n.14596+20_14596+21delinsGT
XM_017012006.2:c.7501+20_7501+21delinsGT	XP_016867495.1:n.7501+20_7501+21delinsGT
XM_017012007.1:c.7474+20_7474+21delinsGT	XP_016867496.1:n.7474+20_7474+21delinsGT
XR_001744643.2:n.16165+20_16165+21delinsGT
NM_033026.6:c.14596+20_14596+21delinsGT MANE Select	NP_149015.2:n.14596+20_14596+21delinsGT
NM_014510.3:c.14596+20_14596+21delinsGT	NP_055325.2:n.14596+20_14596+21delinsGT