Canonical Allele Identifier: CA1926177122

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967666_87967669delinsATTG , CM000672.2:g.87967666_87967669delinsATTG	GRCh38
NC_000010.10:g.89727423_89727426delinsATTG , CM000672.1:g.89727423_89727426delinsATTG	GRCh37
NC_000010.9:g.89717403_89717406delinsATTG	NCBI36
NG_007466.2:g.109228_109231delinsATTG , LRG_311:g.109228_109231delinsATTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*2435_*2438delinsATTG	ENSP00000518161.1:n.*2435_*2438delinsATTG...
ENST00000688158.2:n.4141_4144delinsATTG
ENST00000706954.1:c.*2194_*2197delinsATTG	ENSP00000516674.1:n.*2194_*2197delinsATTG...
ENST00000706955.1:c.*3441_*3444delinsATTG	ENSP00000516675.1:n.*3441_*3444delinsATTG...
ENST00000688158.1:c.*3517_*3520delinsATTG	ENSP00000509254.1:n.*3517_*3520delinsATTG...
ENST00000693560.1:c.*2194_*2197delinsATTG	ENSP00000509861.1:n.*2194_*2197delinsATTG...
ENST00000371953.8:c.*2194_*2197delinsATTG MANE Select	ENSP00000361021.3:n.*2194_*2197delinsATTG...
ENST00000371953.7:c.*2194_*2197delinsATTG	ENSP00000361021.3:n.*2194_*2197delinsATTG...
NM_000314.5:c.*2194_*2197delinsATTG	NP_000305.3:n.*2194_*2197delinsATTG
NM_000314.6:c.*2194_*2197delinsATTG	NP_000305.3:n.*2194_*2197delinsATTG
NM_001304717.2:c.*2194_*2197delinsATTG	NP_001291646.2:n.*2194_*2197delinsATTG
NM_001304718.1:c.*2194_*2197delinsATTG	NP_001291647.1:n.*2194_*2197delinsATTG
XM_006717926.2:c.*2194_*2197delinsATTG	XP_006717989.1:n.*2194_*2197delinsATTG
XM_011539982.1:c.*2194_*2197delinsATTG	XP_011538284.1:n.*2194_*2197delinsATTG
XR_945791.1:n.3976_3979delinsATTG
NM_000314.7:c.*2194_*2197delinsATTG	NP_000305.3:n.*2194_*2197delinsATTG
NM_001304717.5:c.*2194_*2197delinsATTG	NP_001291646.4:n.*2194_*2197delinsATTG
NM_001304718.2:c.*2194_*2197delinsATTG	NP_001291647.1:n.*2194_*2197delinsATTG
NM_000314.8:c.*2194_*2197delinsATTG MANE Select	NP_000305.3:n.*2194_*2197delinsATTG