Canonical Allele Identifier: CA1926182607

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952152_87952159delinsATTATTAT , CM000672.2:g.87952152_87952159delinsATTATTAT	GRCh38
NC_000010.10:g.89711909_89711916delinsATTATTAT , CM000672.1:g.89711909_89711916delinsATTATTAT	GRCh37
NC_000010.9:g.89701889_89701896delinsATTATTAT	NCBI36
NG_007466.2:g.93714_93721delinsATTATTAT , LRG_311:g.93714_93721delinsATTATTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.527_534delinsATTATTAT	ENSP00000514759.2:p.Tyr176=
ENST00000710265.1:c.527_534delinsATTATTAT	ENSP00000518161.1:p.Tyr176=
ENST00000472832.3:c.527_534delinsATTATTAT	ENSP00000483066.2:p.Tyr176=
ENST00000688158.2:n.1262_1269delinsATTATTAT
ENST00000688922.2:c.*357_*364delinsATTATTAT	ENSP00000508742.2:n.*357_*364delinsATTATTAT
ENST00000700021.1:c.482_489delinsATTATTAT	ENSP00000514757.1:p.Tyr161=
ENST00000700022.1:c.493-5701_493-5694delinsATTATTAT	ENSP00000514758.1:n.493-5701_493-5694delinsATTATTAT
ENST00000700023.1:n.1685_1692delinsATTATTAT
ENST00000700024.1:n.1919_1926delinsATTATTAT
ENST00000700025.1:n.1296_1303delinsATTATTAT
ENST00000700029.1:c.361_368delinsATTATTAT
ENST00000706954.1:c.527_534delinsATTATTAT	ENSP00000516674.1:p.Tyr176=
ENST00000706955.1:c.*562_*569delinsATTATTAT	ENSP00000516675.1:n.*562_*569delinsATTATTAT
ENST00000686459.1:c.*113_*120delinsATTATTAT	ENSP00000508909.1:n.*113_*120delinsATTATTAT
ENST00000688158.1:c.*638_*645delinsATTATTAT	ENSP00000509254.1:n.*638_*645delinsATTATTAT
ENST00000688308.1:c.527_534delinsATTATTAT	ENSP00000508752.1:p.Tyr176=
ENST00000688922.1:c.448_455delinsATTATTAT
ENST00000693560.1:c.1046_1053delinsATTATTAT	ENSP00000509861.1:p.Tyr349=
ENST00000371953.8:c.527_534delinsATTATTAT MANE Select	ENSP00000361021.3:p.Tyr176=
ENST00000371953.7:c.527_534delinsATTATTAT	ENSP00000361021.3:p.Tyr176=
NM_000314.5:c.527_534delinsATTATTAT	NP_000305.3:p.Tyr176=
NM_000314.6:c.527_534delinsATTATTAT	NP_000305.3:p.Tyr176=
NM_001304717.2:c.1046_1053delinsATTATTAT	NP_001291646.2:p.Tyr349=
NM_001304718.1:c.-65_-58delinsATTATTAT	NP_001291647.1:n.-65_-58delinsATTATTAT
XM_006717926.2:c.482_489delinsATTATTAT	XP_006717989.1:p.Tyr161=
XM_011539981.1:c.527_534delinsATTATTAT	XP_011538283.1:p.Tyr176=
XM_011539982.1:c.431_438delinsATTATTAT	XP_011538284.1:p.Tyr144=
XR_945789.1:n.1398_1405delinsATTATTAT
XR_945790.1:n.1515_1522delinsATTATTAT
XR_945791.1:n.1205-5701_1205-5694delinsATTATTAT
NM_000314.7:c.527_534delinsATTATTAT	NP_000305.3:p.Tyr176=
NM_001304717.5:c.1046_1053delinsATTATTAT	NP_001291646.4:p.Tyr349=
NM_001304718.2:c.-65_-58delinsATTATTAT	NP_001291647.1:n.-65_-58delinsATTATTAT
NM_000314.8:c.527_534delinsATTATTAT MANE Select	NP_000305.3:p.Tyr176=