Canonical Allele Identifier: CA4320059

Gene: PCLO

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.82952175_82952177dup , CM000669.2:g.82952175_82952177dup	GRCh38
NC_000007.13:g.82581491_82581493dup , CM000669.1:g.82581491_82581493dup	GRCh37
NC_000007.12:g.82419427_82419429dup	NCBI36
NG_047145.1:g.215707_215709dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333891.14:c.8778_8780dup MANE Select	ENSP00000334319.8:p.Asp2926_Glu2927insAsp
ENST00000333891.13:c.8778_8780dup	ENSP00000334319.8:p.Asp2926_Glu2927insAsp
ENST00000423517.6:c.8778_8780dup	ENSP00000388393.2:p.Asp2926_Glu2927insAsp
NM_014510.2:c.8778_8780dup	NP_055325.2:p.Asp2926_Glu2927insAsp
NM_033026.5:c.8778_8780dup	NP_149015.2:p.Asp2926_Glu2927insAsp
XM_017012006.2:c.4017+13596_4017+13598dup	XP_016867495.1:n.4017+13596_4017+13598dup
XM_017012007.1:c.4017+13596_4017+13598dup	XP_016867496.1:n.4017+13596_4017+13598dup
XR_001744643.2:n.10347_10349dup
NM_033026.6:c.8778_8780dup MANE Select	NP_149015.2:p.Asp2926_Glu2927insAsp
NM_014510.3:c.8778_8780dup	NP_055325.2:p.Asp2926_Glu2927insAsp