Canonical Allele Identifier: CA891841267

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961035_87961036delinsCC , CM000672.2:g.87961035_87961036delinsCC	GRCh38
NC_000010.10:g.89720792_89720793delinsCC , CM000672.1:g.89720792_89720793delinsCC	GRCh37
NC_000010.9:g.89710772_89710773delinsCC	NCBI36
NG_007466.2:g.102597_102598delinsCC , LRG_311:g.102597_102598delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1036_1037delinsCC	ENSP00000514759.2:p.Tyr346Pro
ENST00000710265.1:c.943_944delinsCC	ENSP00000518161.1:p.Tyr315Pro
ENST00000472832.3:c.943_944delinsCC	ENSP00000483066.2:p.Tyr315Pro
ENST00000688158.2:n.1678_1679delinsCC
ENST00000688922.2:c.*773_*774delinsCC	ENSP00000508742.2:n.*773_*774delinsCC
ENST00000700021.1:c.898_899delinsCC	ENSP00000514757.1:p.Tyr300Pro
ENST00000700022.1:c.*282_*283delinsCC	ENSP00000514758.1:n.*282_*283delinsCC
ENST00000700023.1:n.2101_2102delinsCC
ENST00000700024.1:n.2335_2336delinsCC
ENST00000700025.1:n.1712_1713delinsCC
ENST00000700026.1:n.580_581delinsCC
ENST00000706954.1:c.943_944delinsCC	ENSP00000516674.1:p.Tyr315Pro
ENST00000706955.1:c.*978_*979delinsCC	ENSP00000516675.1:n.*978_*979delinsCC
ENST00000686459.1:c.*529_*530delinsCC	ENSP00000508909.1:n.*529_*530delinsCC
ENST00000688158.1:c.*1054_*1055delinsCC	ENSP00000509254.1:n.*1054_*1055delinsCC
ENST00000688308.1:c.943_944delinsCC	ENSP00000508752.1:p.Tyr315Pro
ENST00000688922.1:c.864_865delinsCC
ENST00000693560.1:c.1462_1463delinsCC	ENSP00000509861.1:p.Tyr488Pro
ENST00000371953.8:c.943_944delinsCC MANE Select	ENSP00000361021.3:p.Tyr315Pro
ENST00000371953.7:c.943_944delinsCC	ENSP00000361021.3:p.Tyr315Pro
ENST00000472832.2:c.370_371delinsCC	ENSP00000483066.1:p.Tyr124Pro
NM_000314.5:c.943_944delinsCC	NP_000305.3:p.Tyr315Pro
NM_000314.6:c.943_944delinsCC	NP_000305.3:p.Tyr315Pro
NM_001304717.2:c.1462_1463delinsCC	NP_001291646.2:p.Tyr488Pro
NM_001304718.1:c.352_353delinsCC	NP_001291647.1:p.Tyr118Pro
XM_006717926.2:c.898_899delinsCC	XP_006717989.1:p.Tyr300Pro
XM_011539981.1:c.943_944delinsCC	XP_011538283.1:p.Tyr315Pro
XM_011539982.1:c.847_848delinsCC	XP_011538284.1:p.Tyr283Pro
XR_945791.1:n.1513_1514delinsCC
NM_000314.7:c.943_944delinsCC	NP_000305.3:p.Tyr315Pro
NM_001304717.5:c.1462_1463delinsCC	NP_001291646.4:p.Tyr488Pro
NM_001304718.2:c.352_353delinsCC	NP_001291647.1:p.Tyr118Pro
NM_000314.8:c.943_944delinsCC MANE Select	NP_000305.3:p.Tyr315Pro