Canonical Allele Identifier: CA1721404312

Gene: PCLO

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82824218_82824222delinsTAAAA , CM000669.2:g.82824218_82824222delinsTAAAA	GRCh38
NC_000007.13:g.82453534_82453538delinsTAAAA , CM000669.1:g.82453534_82453538delinsTAAAA	GRCh37
NC_000007.12:g.82291470_82291474delinsTAAAA	NCBI36
NG_047145.1:g.343660_343664delinsTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333891.14:c.14596+14_14596+18delinsTTTTA MANE Select	ENSP00000334319.8:n.14596+14_14596+18delinsTTTTA
ENST00000333891.13:c.14596+14_14596+18delinsTTTTA	ENSP00000334319.8:n.14596+14_14596+18delinsTTTTA
ENST00000423517.6:c.14596+14_14596+18delinsTTTTA	ENSP00000388393.2:n.14596+14_14596+18delinsTTTTA
ENST00000426442.6:n.1091+14_1091+18delinsTTTTA
ENST00000618073.1:c.859+14_859+18delinsTTTTA	ENSP00000482390.1:n.859+14_859+18delinsTTTTA
NM_014510.2:c.14596+14_14596+18delinsTTTTA	NP_055325.2:n.14596+14_14596+18delinsTTTTA
NM_033026.5:c.14596+14_14596+18delinsTTTTA	NP_149015.2:n.14596+14_14596+18delinsTTTTA
XM_017012006.2:c.7501+14_7501+18delinsTTTTA	XP_016867495.1:n.7501+14_7501+18delinsTTTTA
XM_017012007.1:c.7474+14_7474+18delinsTTTTA	XP_016867496.1:n.7474+14_7474+18delinsTTTTA
XR_001744643.2:n.16165+14_16165+18delinsTTTTA
NM_033026.6:c.14596+14_14596+18delinsTTTTA MANE Select	NP_149015.2:n.14596+14_14596+18delinsTTTTA
NM_014510.3:c.14596+14_14596+18delinsTTTTA	NP_055325.2:n.14596+14_14596+18delinsTTTTA