Canonical Allele Identifier: CA891841652

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965419_87965420delinsGG , CM000672.2:g.87965419_87965420delinsGG	GRCh38
NC_000010.10:g.89725176_89725177delinsGG , CM000672.1:g.89725176_89725177delinsGG	GRCh37
NC_000010.9:g.89715156_89715157delinsGG	NCBI36
NG_007466.2:g.106981_106982delinsGG , LRG_311:g.106981_106982delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1252_1253delinsGG	ENSP00000514759.2:p.Pro418Gly
ENST00000710265.1:c.*188_*189delinsGG	ENSP00000518161.1:n.*188_*189delinsGG
ENST00000688158.2:n.1894_1895delinsGG
ENST00000688922.2:c.*989_*990delinsGG	ENSP00000508742.2:n.*989_*990delinsGG
ENST00000700021.1:c.1114_1115delinsGG	ENSP00000514757.1:p.Pro372Gly
ENST00000700022.1:c.*498_*499delinsGG	ENSP00000514758.1:n.*498_*499delinsGG
ENST00000700023.1:n.2317_2318delinsGG
ENST00000700024.1:n.2551_2552delinsGG
ENST00000706954.1:c.1159_1160delinsGG	ENSP00000516674.1:p.Pro387Gly
ENST00000706955.1:c.*1194_*1195delinsGG	ENSP00000516675.1:n.*1194_*1195delinsGG
ENST00000686459.1:c.*745_*746delinsGG	ENSP00000508909.1:n.*745_*746delinsGG
ENST00000688158.1:c.*1270_*1271delinsGG	ENSP00000509254.1:n.*1270_*1271delinsGG
ENST00000688308.1:c.1159_1160delinsGG	ENSP00000508752.1:p.Pro387Gly
ENST00000688922.1:c.1080_1081delinsGG
ENST00000693560.1:c.1678_1679delinsGG	ENSP00000509861.1:p.Pro560Gly
ENST00000371953.8:c.1159_1160delinsGG MANE Select	ENSP00000361021.3:p.Pro387Gly
ENST00000371953.7:c.1159_1160delinsGG	ENSP00000361021.3:p.Pro387Gly
NM_000314.5:c.1159_1160delinsGG	NP_000305.3:p.Pro387Gly
NM_000314.6:c.1159_1160delinsGG	NP_000305.3:p.Pro387Gly
NM_001304717.2:c.1678_1679delinsGG	NP_001291646.2:p.Pro560Gly
NM_001304718.1:c.568_569delinsGG	NP_001291647.1:p.Pro190Gly
XM_006717926.2:c.1114_1115delinsGG	XP_006717989.1:p.Pro372Gly
XM_011539982.1:c.1063_1064delinsGG	XP_011538284.1:p.Pro355Gly
XR_945791.1:n.1729_1730delinsGG
NM_000314.7:c.1159_1160delinsGG	NP_000305.3:p.Pro387Gly
NM_001304717.5:c.1678_1679delinsGG	NP_001291646.4:p.Pro560Gly
NM_001304718.2:c.568_569delinsGG	NP_001291647.1:p.Pro190Gly
NM_000314.8:c.1159_1160delinsGG MANE Select	NP_000305.3:p.Pro387Gly