Canonical Allele Identifier: CA2579926742

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960919_87960921del , CM000672.2:g.87960919_87960921del	GRCh38
NC_000010.10:g.89720676_89720678del , CM000672.1:g.89720676_89720678del	GRCh37
NC_000010.9:g.89710656_89710658del	NCBI36
NG_007466.2:g.102481_102483del , LRG_311:g.102481_102483del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.920_922del	ENSP00000514759.2:p.Asn307del
ENST00000710265.1:c.827_829del	ENSP00000518161.1:p.Asn276del
ENST00000472832.3:c.827_829del	ENSP00000483066.2:p.Asn276del
ENST00000688158.2:n.1562_1564del
ENST00000688922.2:c.*657_*659del	ENSP00000508742.2:n.*657_*659del
ENST00000700021.1:c.782_784del	ENSP00000514757.1:p.Asn261del
ENST00000700022.1:c.*166_*168del	ENSP00000514758.1:n.*166_*168del
ENST00000700023.1:n.1985_1987del
ENST00000700024.1:n.2219_2221del
ENST00000700025.1:n.1596_1598del
ENST00000700026.1:n.464_466del
ENST00000700029.1:c.754_756del
ENST00000706954.1:c.827_829del	ENSP00000516674.1:p.Asn276del
ENST00000706955.1:c.*862_*864del	ENSP00000516675.1:n.*862_*864del
ENST00000686459.1:c.*413_*415del	ENSP00000508909.1:n.*413_*415del
ENST00000688158.1:c.*938_*940del	ENSP00000509254.1:n.*938_*940del
ENST00000688308.1:c.827_829del	ENSP00000508752.1:p.Asn276del
ENST00000688922.1:c.748_750del
ENST00000693560.1:c.1346_1348del	ENSP00000509861.1:p.Asn449del
ENST00000371953.8:c.827_829del MANE Select	ENSP00000361021.3:p.Asn276del
ENST00000371953.7:c.827_829del	ENSP00000361021.3:p.Asn276del
ENST00000472832.2:c.254_256del	ENSP00000483066.1:p.Asn85del
NM_000314.5:c.827_829del	NP_000305.3:p.Asn276del
NM_000314.6:c.827_829del	NP_000305.3:p.Asn276del
NM_001304717.2:c.1346_1348del	NP_001291646.2:p.Asn449del
NM_001304718.1:c.236_238del	NP_001291647.1:p.Asn79del
XM_006717926.2:c.782_784del	XP_006717989.1:p.Asn261del
XM_011539981.1:c.827_829del	XP_011538283.1:p.Asn276del
XM_011539982.1:c.731_733del	XP_011538284.1:p.Asn244del
XR_945791.1:n.1397_1399del
NM_000314.7:c.827_829del	NP_000305.3:p.Asn276del
NM_001304717.5:c.1346_1348del	NP_001291646.4:p.Asn449del
NM_001304718.2:c.236_238del	NP_001291647.1:p.Asn79del
NM_000314.8:c.827_829del MANE Select	NP_000305.3:p.Asn276del