Canonical Allele Identifier: CA891841318

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952160_87952162delinsAGC , CM000672.2:g.87952160_87952162delinsAGC	GRCh38
NC_000010.10:g.89711917_89711919delinsAGC , CM000672.1:g.89711917_89711919delinsAGC	GRCh37
NC_000010.9:g.89701897_89701899delinsAGC	NCBI36
NG_007466.2:g.93722_93724delinsAGC , LRG_311:g.93722_93724delinsAGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.535_537delinsAGC	ENSP00000514759.2:p.Ser179=
ENST00000710265.1:c.535_537delinsAGC	ENSP00000518161.1:p.Ser179=
ENST00000472832.3:c.535_537delinsAGC	ENSP00000483066.2:p.Ser179=
ENST00000688158.2:n.1270_1272delinsAGC
ENST00000688922.2:c.*365_*367delinsAGC	ENSP00000508742.2:n.*365_*367delinsAGC
ENST00000700021.1:c.490_492delinsAGC	ENSP00000514757.1:p.Ser164=
ENST00000700022.1:c.493-5693_493-5691delinsAGC	ENSP00000514758.1:n.493-5693_493-5691deli...
ENST00000700023.1:n.1693_1695delinsAGC
ENST00000700024.1:n.1927_1929delinsAGC
ENST00000700025.1:n.1304_1306delinsAGC
ENST00000700029.1:c.369_371delinsAGC
ENST00000706954.1:c.535_537delinsAGC	ENSP00000516674.1:p.Ser179=
ENST00000706955.1:c.*570_*572delinsAGC	ENSP00000516675.1:n.*570_*572delinsAGC
ENST00000686459.1:c.*121_*123delinsAGC	ENSP00000508909.1:n.*121_*123delinsAGC
ENST00000688158.1:c.*646_*648delinsAGC	ENSP00000509254.1:n.*646_*648delinsAGC
ENST00000688308.1:c.535_537delinsAGC	ENSP00000508752.1:p.Ser179=
ENST00000688922.1:c.456_458delinsAGC
ENST00000693560.1:c.1054_1056delinsAGC	ENSP00000509861.1:p.Ser352=
ENST00000371953.8:c.535_537delinsAGC MANE Select	ENSP00000361021.3:p.Ser179=
ENST00000371953.7:c.535_537delinsAGC	ENSP00000361021.3:p.Ser179=
NM_000314.5:c.535_537delinsAGC	NP_000305.3:p.Ser179=
NM_000314.6:c.535_537delinsAGC	NP_000305.3:p.Ser179=
NM_001304717.2:c.1054_1056delinsAGC	NP_001291646.2:p.Ser352=
NM_001304718.1:c.-57_-55delinsAGC	NP_001291647.1:n.-57_-55delinsAGC
XM_006717926.2:c.490_492delinsAGC	XP_006717989.1:p.Ser164=
XM_011539981.1:c.535_537delinsAGC	XP_011538283.1:p.Ser179=
XM_011539982.1:c.439_441delinsAGC	XP_011538284.1:p.Ser147=
XR_945789.1:n.1406_1408delinsAGC
XR_945790.1:n.1523_1525delinsAGC
XR_945791.1:n.1205-5693_1205-5691delinsAGC
NM_000314.7:c.535_537delinsAGC	NP_000305.3:p.Ser179=
NM_001304717.5:c.1054_1056delinsAGC	NP_001291646.4:p.Ser352=
NM_001304718.2:c.-57_-55delinsAGC	NP_001291647.1:n.-57_-55delinsAGC
NM_000314.8:c.535_537delinsAGC MANE Select	NP_000305.3:p.Ser179=