Canonical Allele Identifier: CA891841048

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960927_87960928delinsAA , CM000672.2:g.87960927_87960928delinsAA	GRCh38
NC_000010.10:g.89720684_89720685delinsAA , CM000672.1:g.89720684_89720685delinsAA	GRCh37
NC_000010.9:g.89710664_89710665delinsAA	NCBI36
NG_007466.2:g.102489_102490delinsAA , LRG_311:g.102489_102490delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.928_929delinsAA	ENSP00000514759.2:p.Phe310Asn
ENST00000710265.1:c.835_836delinsAA	ENSP00000518161.1:p.Phe279Asn
ENST00000472832.3:c.835_836delinsAA	ENSP00000483066.2:p.Phe279Asn
ENST00000688158.2:n.1570_1571delinsAA
ENST00000688922.2:c.*665_*666delinsAA	ENSP00000508742.2:n.*665_*666delinsAA
ENST00000700021.1:c.790_791delinsAA	ENSP00000514757.1:p.Phe264Asn
ENST00000700022.1:c.*174_*175delinsAA	ENSP00000514758.1:n.*174_*175delinsAA
ENST00000700023.1:n.1993_1994delinsAA
ENST00000700024.1:n.2227_2228delinsAA
ENST00000700025.1:n.1604_1605delinsAA
ENST00000700026.1:n.472_473delinsAA
ENST00000700029.1:c.762_763delinsAA
ENST00000706954.1:c.835_836delinsAA	ENSP00000516674.1:p.Phe279Asn
ENST00000706955.1:c.*870_*871delinsAA	ENSP00000516675.1:n.*870_*871delinsAA
ENST00000686459.1:c.*421_*422delinsAA	ENSP00000508909.1:n.*421_*422delinsAA
ENST00000688158.1:c.*946_*947delinsAA	ENSP00000509254.1:n.*946_*947delinsAA
ENST00000688308.1:c.835_836delinsAA	ENSP00000508752.1:p.Phe279Asn
ENST00000688922.1:c.756_757delinsAA
ENST00000693560.1:c.1354_1355delinsAA	ENSP00000509861.1:p.Phe452Asn
ENST00000371953.8:c.835_836delinsAA MANE Select	ENSP00000361021.3:p.Phe279Asn
ENST00000371953.7:c.835_836delinsAA	ENSP00000361021.3:p.Phe279Asn
ENST00000472832.2:c.262_263delinsAA	ENSP00000483066.1:p.Phe88Asn
NM_000314.5:c.835_836delinsAA	NP_000305.3:p.Phe279Asn
NM_000314.6:c.835_836delinsAA	NP_000305.3:p.Phe279Asn
NM_001304717.2:c.1354_1355delinsAA	NP_001291646.2:p.Phe452Asn
NM_001304718.1:c.244_245delinsAA	NP_001291647.1:p.Phe82Asn
XM_006717926.2:c.790_791delinsAA	XP_006717989.1:p.Phe264Asn
XM_011539981.1:c.835_836delinsAA	XP_011538283.1:p.Phe279Asn
XM_011539982.1:c.739_740delinsAA	XP_011538284.1:p.Phe247Asn
XR_945791.1:n.1405_1406delinsAA
NM_000314.7:c.835_836delinsAA	NP_000305.3:p.Phe279Asn
NM_001304717.5:c.1354_1355delinsAA	NP_001291646.4:p.Phe452Asn
NM_001304718.2:c.244_245delinsAA	NP_001291647.1:p.Phe82Asn
NM_000314.8:c.835_836delinsAA MANE Select	NP_000305.3:p.Phe279Asn