Canonical Allele Identifier: CA891840418

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957870_87957871delinsGA , CM000672.2:g.87957870_87957871delinsGA	GRCh38
NC_000010.10:g.89717627_89717628delinsGA , CM000672.1:g.89717627_89717628delinsGA	GRCh37
NC_000010.9:g.89707607_89707608delinsGA	NCBI36
NG_007466.2:g.99432_99433delinsGA , LRG_311:g.99432_99433delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.652_653delinsGA	ENSP00000514759.2:p.Cys218Asp
ENST00000710265.1:c.652_653delinsGA	ENSP00000518161.1:p.Cys218Asp
ENST00000472832.3:c.652_653delinsGA	ENSP00000483066.2:p.Cys218Asp
ENST00000688158.2:n.1387_1388delinsGA
ENST00000688922.2:c.*482_*483delinsGA	ENSP00000508742.2:n.*482_*483delinsGA
ENST00000700021.1:c.607_608delinsGA	ENSP00000514757.1:p.Cys203Asp
ENST00000700022.1:c.510_511delinsGA	ENSP00000514758.1:p.Ala171Thr
ENST00000700023.1:n.1810_1811delinsGA
ENST00000700024.1:n.2044_2045delinsGA
ENST00000700025.1:n.1421_1422delinsGA
ENST00000700026.1:n.289_290delinsGA
ENST00000700029.1:c.486_487delinsGA
ENST00000706954.1:c.652_653delinsGA	ENSP00000516674.1:p.Cys218Asp
ENST00000706955.1:c.*687_*688delinsGA	ENSP00000516675.1:n.*687_*688delinsGA
ENST00000686459.1:c.*238_*239delinsGA	ENSP00000508909.1:n.*238_*239delinsGA
ENST00000688158.1:c.*763_*764delinsGA	ENSP00000509254.1:n.*763_*764delinsGA
ENST00000688308.1:c.652_653delinsGA	ENSP00000508752.1:p.Cys218Asp
ENST00000688922.1:c.573_574delinsGA
ENST00000693560.1:c.1171_1172delinsGA	ENSP00000509861.1:p.Cys391Asp
ENST00000371953.8:c.652_653delinsGA MANE Select	ENSP00000361021.3:p.Cys218Asp
ENST00000371953.7:c.652_653delinsGA	ENSP00000361021.3:p.Cys218Asp
ENST00000472832.2:c.79_80delinsGA	ENSP00000483066.1:p.Cys27Asp
NM_000314.5:c.652_653delinsGA	NP_000305.3:p.Cys218Asp
NM_000314.6:c.652_653delinsGA	NP_000305.3:p.Cys218Asp
NM_001304717.2:c.1171_1172delinsGA	NP_001291646.2:p.Cys391Asp
NM_001304718.1:c.61_62delinsGA	NP_001291647.1:p.Cys21Asp
XM_006717926.2:c.607_608delinsGA	XP_006717989.1:p.Cys203Asp
XM_011539981.1:c.652_653delinsGA	XP_011538283.1:p.Cys218Asp
XM_011539982.1:c.556_557delinsGA	XP_011538284.1:p.Cys186Asp
XR_945791.1:n.1222_1223delinsGA
NM_000314.7:c.652_653delinsGA	NP_000305.3:p.Cys218Asp
NM_001304717.5:c.1171_1172delinsGA	NP_001291646.4:p.Cys391Asp
NM_001304718.2:c.61_62delinsGA	NP_001291647.1:p.Cys21Asp
NM_000314.8:c.652_653delinsGA MANE Select	NP_000305.3:p.Cys218Asp