Canonical Allele Identifier: CA891836412

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961035_87961036delinsGG , CM000672.2:g.87961035_87961036delinsGG	GRCh38
NC_000010.10:g.89720792_89720793delinsGG , CM000672.1:g.89720792_89720793delinsGG	GRCh37
NC_000010.9:g.89710772_89710773delinsGG	NCBI36
NG_007466.2:g.102597_102598delinsGG , LRG_311:g.102597_102598delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1036_1037delinsGG	ENSP00000514759.2:p.Tyr346Gly
ENST00000710265.1:c.943_944delinsGG	ENSP00000518161.1:p.Tyr315Gly
ENST00000472832.3:c.943_944delinsGG	ENSP00000483066.2:p.Tyr315Gly
ENST00000688158.2:n.1678_1679delinsGG
ENST00000688922.2:c.*773_*774delinsGG	ENSP00000508742.2:n.*773_*774delinsGG
ENST00000700021.1:c.898_899delinsGG	ENSP00000514757.1:p.Tyr300Gly
ENST00000700022.1:c.*282_*283delinsGG	ENSP00000514758.1:n.*282_*283delinsGG
ENST00000700023.1:n.2101_2102delinsGG
ENST00000700024.1:n.2335_2336delinsGG
ENST00000700025.1:n.1712_1713delinsGG
ENST00000700026.1:n.580_581delinsGG
ENST00000706954.1:c.943_944delinsGG	ENSP00000516674.1:p.Tyr315Gly
ENST00000706955.1:c.*978_*979delinsGG	ENSP00000516675.1:n.*978_*979delinsGG
ENST00000686459.1:c.*529_*530delinsGG	ENSP00000508909.1:n.*529_*530delinsGG
ENST00000688158.1:c.*1054_*1055delinsGG	ENSP00000509254.1:n.*1054_*1055delinsGG
ENST00000688308.1:c.943_944delinsGG	ENSP00000508752.1:p.Tyr315Gly
ENST00000688922.1:c.864_865delinsGG
ENST00000693560.1:c.1462_1463delinsGG	ENSP00000509861.1:p.Tyr488Gly
ENST00000371953.8:c.943_944delinsGG MANE Select	ENSP00000361021.3:p.Tyr315Gly
ENST00000371953.7:c.943_944delinsGG	ENSP00000361021.3:p.Tyr315Gly
ENST00000472832.2:c.370_371delinsGG	ENSP00000483066.1:p.Tyr124Gly
NM_000314.5:c.943_944delinsGG	NP_000305.3:p.Tyr315Gly
NM_000314.6:c.943_944delinsGG	NP_000305.3:p.Tyr315Gly
NM_001304717.2:c.1462_1463delinsGG	NP_001291646.2:p.Tyr488Gly
NM_001304718.1:c.352_353delinsGG	NP_001291647.1:p.Tyr118Gly
XM_006717926.2:c.898_899delinsGG	XP_006717989.1:p.Tyr300Gly
XM_011539981.1:c.943_944delinsGG	XP_011538283.1:p.Tyr315Gly
XM_011539982.1:c.847_848delinsGG	XP_011538284.1:p.Tyr283Gly
XR_945791.1:n.1513_1514delinsGG
NM_000314.7:c.943_944delinsGG	NP_000305.3:p.Tyr315Gly
NM_001304717.5:c.1462_1463delinsGG	NP_001291646.4:p.Tyr488Gly
NM_001304718.2:c.352_353delinsGG	NP_001291647.1:p.Tyr118Gly
NM_000314.8:c.943_944delinsGG MANE Select	NP_000305.3:p.Tyr315Gly