Canonical Allele Identifier: CA2788898395

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965501_87965502insAAACCAAACACACCCAACA , CM000672.2:g.87965501_87965502insAAACCAAACACACCCAACA	GRCh38
NC_000010.10:g.89725258_89725259insAAACCAAACACACCCAACA , CM000672.1:g.89725258_89725259insAAACCAAACACACCCAACA	GRCh37
NC_000010.9:g.89715238_89715239insAAACCAAACACACCCAACA	NCBI36
NG_007466.2:g.107063_107064insAAACCAAACACACCCAACA , LRG_311:g.107063_107064insAAACCAAACACACCCAACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*29_*30insAAACCAAACACACCCAACA	ENSP00000514759.2:n.*29_*30insAAACCAAACACACCCAACA
ENST00000710265.1:c.*270_*271insAAACCAAACACACCCAACA	ENSP00000518161.1:n.*270_*271insAAACCAAACACACCCAACA
ENST00000688158.2:n.1976_1977insAAACCAAACACACCCAACA
ENST00000688922.2:c.*1071_*1072insAAACCAAACACACCCAACA	ENSP00000508742.2:n.*1071_*1072insAAACCAAACACACCCAACA
ENST00000700021.1:c.*29_*30insAAACCAAACACACCCAACA	ENSP00000514757.1:n.*29_*30insAAACCAAACACACCCAACA
ENST00000700022.1:c.*580_*581insAAACCAAACACACCCAACA	ENSP00000514758.1:n.*580_*581insAAACCAAACACACCCAACA
ENST00000700023.1:n.2399_2400insAAACCAAACACACCCAACA
ENST00000700024.1:n.2633_2634insAAACCAAACACACCCAACA
ENST00000706954.1:c.*29_*30insAAACCAAACACACCCAACA	ENSP00000516674.1:n.*29_*30insAAACCAAACACACCCAACA
ENST00000706955.1:c.*1276_*1277insAAACCAAACACACCCAACA	ENSP00000516675.1:n.*1276_*1277insAAACCAAACACACCCAACA
ENST00000686459.1:c.*827_*828insAAACCAAACACACCCAACA	ENSP00000508909.1:n.*827_*828insAAACCAAACACACCCAACA
ENST00000688158.1:c.*1352_*1353insAAACCAAACACACCCAACA	ENSP00000509254.1:n.*1352_*1353insAAACCAAACACACCCAACA
ENST00000688308.1:c.*29_*30insAAACCAAACACACCCAACA	ENSP00000508752.1:n.*29_*30insAAACCAAACACACCCAACA
ENST00000688922.1:c.1162_1163insAAACCAAACACACCCAACA
ENST00000693560.1:c.*29_*30insAAACCAAACACACCCAACA	ENSP00000509861.1:n.*29_*30insAAACCAAACACACCCAACA
ENST00000371953.8:c.*29_*30insAAACCAAACACACCCAACA MANE Select	ENSP00000361021.3:n.*29_*30insAAACCAAACACACCCAACA
ENST00000371953.7:c.*29_*30insAAACCAAACACACCCAACA	ENSP00000361021.3:n.*29_*30insAAACCAAACACACCCAACA
NM_000314.5:c.*29_*30insAAACCAAACACACCCAACA	NP_000305.3:n.*29_*30insAAACCAAACACACCCAACA
NM_000314.6:c.*29_*30insAAACCAAACACACCCAACA	NP_000305.3:n.*29_*30insAAACCAAACACACCCAACA
NM_001304717.2:c.*29_*30insAAACCAAACACACCCAACA	NP_001291646.2:n.*29_*30insAAACCAAACACACCCAACA
NM_001304718.1:c.*29_*30insAAACCAAACACACCCAACA	NP_001291647.1:n.*29_*30insAAACCAAACACACCCAACA
XM_006717926.2:c.*29_*30insAAACCAAACACACCCAACA	XP_006717989.1:n.*29_*30insAAACCAAACACACCCAACA
XM_011539982.1:c.*29_*30insAAACCAAACACACCCAACA	XP_011538284.1:n.*29_*30insAAACCAAACACACCCAACA
XR_945791.1:n.1811_1812insAAACCAAACACACCCAACA
NM_000314.7:c.*29_*30insAAACCAAACACACCCAACA	NP_000305.3:n.*29_*30insAAACCAAACACACCCAACA
NM_001304717.5:c.*29_*30insAAACCAAACACACCCAACA	NP_001291646.4:n.*29_*30insAAACCAAACACACCCAACA
NM_001304718.2:c.*29_*30insAAACCAAACACACCCAACA	NP_001291647.1:n.*29_*30insAAACCAAACACACCCAACA
NM_000314.8:c.*29_*30insAAACCAAACACACCCAACA MANE Select	NP_000305.3:n.*29_*30insAAACCAAACACACCCAACA