Canonical Allele Identifier: CA2578925823

Gene: PCLO

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824213_82824214del , CM000669.2:g.82824213_82824214del	GRCh38
NC_000007.13:g.82453529_82453530del , CM000669.1:g.82453529_82453530del	GRCh37
NC_000007.12:g.82291465_82291466del	NCBI36
NG_047145.1:g.343669_343670del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333891.14:c.14596+23_14596+24del MANE Select	ENSP00000334319.8:n.14596+23_14596+24del
ENST00000333891.13:c.14596+23_14596+24del	ENSP00000334319.8:n.14596+23_14596+24del
ENST00000423517.6:c.14596+23_14596+24del	ENSP00000388393.2:n.14596+23_14596+24del
ENST00000426442.6:n.1091+23_1091+24del
ENST00000618073.1:c.859+23_859+24del	ENSP00000482390.1:n.859+23_859+24del
NM_014510.2:c.14596+23_14596+24del	NP_055325.2:n.14596+23_14596+24del
NM_033026.5:c.14596+23_14596+24del	NP_149015.2:n.14596+23_14596+24del
XM_017012006.2:c.7501+23_7501+24del	XP_016867495.1:n.7501+23_7501+24del
XM_017012007.1:c.7474+23_7474+24del	XP_016867496.1:n.7474+23_7474+24del
XR_001744643.2:n.16165+23_16165+24del
NM_033026.6:c.14596+23_14596+24del MANE Select	NP_149015.2:n.14596+23_14596+24del
NM_014510.3:c.14596+23_14596+24del	NP_055325.2:n.14596+23_14596+24del