Canonical Allele Identifier: CA891837987

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965419_87965421delinsACT , CM000672.2:g.87965419_87965421delinsACT	GRCh38
NC_000010.10:g.89725176_89725178delinsACT , CM000672.1:g.89725176_89725178delinsACT	GRCh37
NC_000010.9:g.89715156_89715158delinsACT	NCBI36
NG_007466.2:g.106981_106983delinsACT , LRG_311:g.106981_106983delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1252_1254delinsACT	ENSP00000514759.2:p.Pro418Thr
ENST00000710265.1:c.*188_*190delinsACT	ENSP00000518161.1:n.*188_*190delinsACT
ENST00000688158.2:n.1894_1896delinsACT
ENST00000688922.2:c.*989_*991delinsACT	ENSP00000508742.2:n.*989_*991delinsACT
ENST00000700021.1:c.1114_1116delinsACT	ENSP00000514757.1:p.Pro372Thr
ENST00000700022.1:c.*498_*500delinsACT	ENSP00000514758.1:n.*498_*500delinsACT
ENST00000700023.1:n.2317_2319delinsACT
ENST00000700024.1:n.2551_2553delinsACT
ENST00000706954.1:c.1159_1161delinsACT	ENSP00000516674.1:p.Pro387Thr
ENST00000706955.1:c.*1194_*1196delinsACT	ENSP00000516675.1:n.*1194_*1196delinsACT
ENST00000686459.1:c.*745_*747delinsACT	ENSP00000508909.1:n.*745_*747delinsACT
ENST00000688158.1:c.*1270_*1272delinsACT	ENSP00000509254.1:n.*1270_*1272delinsACT
ENST00000688308.1:c.1159_1161delinsACT	ENSP00000508752.1:p.Pro387Thr
ENST00000688922.1:c.1080_1082delinsACT
ENST00000693560.1:c.1678_1680delinsACT	ENSP00000509861.1:p.Pro560Thr
ENST00000371953.8:c.1159_1161delinsACT MANE Select	ENSP00000361021.3:p.Pro387Thr
ENST00000371953.7:c.1159_1161delinsACT	ENSP00000361021.3:p.Pro387Thr
NM_000314.5:c.1159_1161delinsACT	NP_000305.3:p.Pro387Thr
NM_000314.6:c.1159_1161delinsACT	NP_000305.3:p.Pro387Thr
NM_001304717.2:c.1678_1680delinsACT	NP_001291646.2:p.Pro560Thr
NM_001304718.1:c.568_570delinsACT	NP_001291647.1:p.Pro190Thr
XM_006717926.2:c.1114_1116delinsACT	XP_006717989.1:p.Pro372Thr
XM_011539982.1:c.1063_1065delinsACT	XP_011538284.1:p.Pro355Thr
XR_945791.1:n.1729_1731delinsACT
NM_000314.7:c.1159_1161delinsACT	NP_000305.3:p.Pro387Thr
NM_001304717.5:c.1678_1680delinsACT	NP_001291646.4:p.Pro560Thr
NM_001304718.2:c.568_570delinsACT	NP_001291647.1:p.Pro190Thr
NM_000314.8:c.1159_1161delinsACT MANE Select	NP_000305.3:p.Pro387Thr