Canonical Allele Identifier: CA1926176997

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967590_87967591delinsAC , CM000672.2:g.87967590_87967591delinsAC	GRCh38
NC_000010.10:g.89727347_89727348delinsAC , CM000672.1:g.89727347_89727348delinsAC	GRCh37
NC_000010.9:g.89717327_89717328delinsAC	NCBI36
NG_007466.2:g.109152_109153delinsAC , LRG_311:g.109152_109153delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*2359_*2360delinsAC	ENSP00000518161.1:n.*2359_*2360delinsAC
ENST00000688158.2:n.4065_4066delinsAC
ENST00000706954.1:c.*2118_*2119delinsAC	ENSP00000516674.1:n.*2118_*2119delinsAC
ENST00000706955.1:c.*3365_*3366delinsAC	ENSP00000516675.1:n.*3365_*3366delinsAC
ENST00000688158.1:c.*3441_*3442delinsAC	ENSP00000509254.1:n.*3441_*3442delinsAC
ENST00000693560.1:c.*2118_*2119delinsAC	ENSP00000509861.1:n.*2118_*2119delinsAC
ENST00000371953.8:c.*2118_*2119delinsAC MANE Select	ENSP00000361021.3:n.*2118_*2119delinsAC
ENST00000371953.7:c.*2118_*2119delinsAC	ENSP00000361021.3:n.*2118_*2119delinsAC
NM_000314.5:c.*2118_*2119delinsAC	NP_000305.3:n.*2118_*2119delinsAC
NM_000314.6:c.*2118_*2119delinsAC	NP_000305.3:n.*2118_*2119delinsAC
NM_001304717.2:c.*2118_*2119delinsAC	NP_001291646.2:n.*2118_*2119delinsAC
NM_001304718.1:c.*2118_*2119delinsAC	NP_001291647.1:n.*2118_*2119delinsAC
XM_006717926.2:c.*2118_*2119delinsAC	XP_006717989.1:n.*2118_*2119delinsAC
XM_011539982.1:c.*2118_*2119delinsAC	XP_011538284.1:n.*2118_*2119delinsAC
XR_945791.1:n.3900_3901delinsAC
NM_000314.7:c.*2118_*2119delinsAC	NP_000305.3:n.*2118_*2119delinsAC
NM_001304717.5:c.*2118_*2119delinsAC	NP_001291646.4:n.*2118_*2119delinsAC
NM_001304718.2:c.*2118_*2119delinsAC	NP_001291647.1:n.*2118_*2119delinsAC
NM_000314.8:c.*2118_*2119delinsAC MANE Select	NP_000305.3:n.*2118_*2119delinsAC