Canonical Allele Identifier: CA891836176

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961017_87961019delinsATT , CM000672.2:g.87961017_87961019delinsATT	GRCh38
NC_000010.10:g.89720774_89720776delinsATT , CM000672.1:g.89720774_89720776delinsATT	GRCh37
NC_000010.9:g.89710754_89710756delinsATT	NCBI36
NG_007466.2:g.102579_102581delinsATT , LRG_311:g.102579_102581delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1018_1020delinsATT	ENSP00000514759.2:p.Ala340Ile
ENST00000710265.1:c.925_927delinsATT	ENSP00000518161.1:p.Ala309Ile
ENST00000472832.3:c.925_927delinsATT	ENSP00000483066.2:p.Ala309Ile
ENST00000688158.2:n.1660_1662delinsATT
ENST00000688922.2:c.*755_*757delinsATT	ENSP00000508742.2:n.*755_*757delinsATT
ENST00000700021.1:c.880_882delinsATT	ENSP00000514757.1:p.Ala294Ile
ENST00000700022.1:c.*264_*266delinsATT	ENSP00000514758.1:n.*264_*266delinsATT
ENST00000700023.1:n.2083_2085delinsATT
ENST00000700024.1:n.2317_2319delinsATT
ENST00000700025.1:n.1694_1696delinsATT
ENST00000700026.1:n.562_564delinsATT
ENST00000706954.1:c.925_927delinsATT	ENSP00000516674.1:p.Ala309Ile
ENST00000706955.1:c.*960_*962delinsATT	ENSP00000516675.1:n.*960_*962delinsATT
ENST00000686459.1:c.*511_*513delinsATT	ENSP00000508909.1:n.*511_*513delinsATT
ENST00000688158.1:c.*1036_*1038delinsATT	ENSP00000509254.1:n.*1036_*1038delinsATT
ENST00000688308.1:c.925_927delinsATT	ENSP00000508752.1:p.Ala309Ile
ENST00000688922.1:c.846_848delinsATT
ENST00000693560.1:c.1444_1446delinsATT	ENSP00000509861.1:p.Ala482Ile
ENST00000371953.8:c.925_927delinsATT MANE Select	ENSP00000361021.3:p.Ala309Ile
ENST00000371953.7:c.925_927delinsATT	ENSP00000361021.3:p.Ala309Ile
ENST00000472832.2:c.352_354delinsATT	ENSP00000483066.1:p.Ala118Ile
NM_000314.5:c.925_927delinsATT	NP_000305.3:p.Ala309Ile
NM_000314.6:c.925_927delinsATT	NP_000305.3:p.Ala309Ile
NM_001304717.2:c.1444_1446delinsATT	NP_001291646.2:p.Ala482Ile
NM_001304718.1:c.334_336delinsATT	NP_001291647.1:p.Ala112Ile
XM_006717926.2:c.880_882delinsATT	XP_006717989.1:p.Ala294Ile
XM_011539981.1:c.925_927delinsATT	XP_011538283.1:p.Ala309Ile
XM_011539982.1:c.829_831delinsATT	XP_011538284.1:p.Ala277Ile
XR_945791.1:n.1495_1497delinsATT
NM_000314.7:c.925_927delinsATT	NP_000305.3:p.Ala309Ile
NM_001304717.5:c.1444_1446delinsATT	NP_001291646.4:p.Ala482Ile
NM_001304718.2:c.334_336delinsATT	NP_001291647.1:p.Ala112Ile
NM_000314.8:c.925_927delinsATT MANE Select	NP_000305.3:p.Ala309Ile