Canonical Allele Identifier: CA891836842

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961077_87961079delinsTGG , CM000672.2:g.87961077_87961079delinsTGG	GRCh38
NC_000010.10:g.89720834_89720836delinsTGG , CM000672.1:g.89720834_89720836delinsTGG	GRCh37
NC_000010.9:g.89710814_89710816delinsTGG	NCBI36
NG_007466.2:g.102639_102641delinsTGG , LRG_311:g.102639_102641delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1078_1080delinsTGG	ENSP00000514759.2:p.Asn360Trp
ENST00000710265.1:c.985_987delinsTGG	ENSP00000518161.1:p.Asn329Trp
ENST00000472832.3:c.985_987delinsTGG	ENSP00000483066.2:p.Asn329Trp
ENST00000688158.2:n.1720_1722delinsTGG
ENST00000688922.2:c.*815_*817delinsTGG	ENSP00000508742.2:n.*815_*817delinsTGG
ENST00000700021.1:c.940_942delinsTGG	ENSP00000514757.1:p.Asn314Trp
ENST00000700022.1:c.*324_*326delinsTGG	ENSP00000514758.1:n.*324_*326delinsTGG
ENST00000700023.1:n.2143_2145delinsTGG
ENST00000700024.1:n.2377_2379delinsTGG
ENST00000700025.1:n.1754_1756delinsTGG
ENST00000700026.1:n.622_624delinsTGG
ENST00000706954.1:c.985_987delinsTGG	ENSP00000516674.1:p.Asn329Trp
ENST00000706955.1:c.*1020_*1022delinsTGG	ENSP00000516675.1:n.*1020_*1022delinsTGG
ENST00000686459.1:c.*571_*573delinsTGG	ENSP00000508909.1:n.*571_*573delinsTGG
ENST00000688158.1:c.*1096_*1098delinsTGG	ENSP00000509254.1:n.*1096_*1098delinsTGG
ENST00000688308.1:c.985_987delinsTGG	ENSP00000508752.1:p.Asn329Trp
ENST00000688922.1:c.906_908delinsTGG
ENST00000693560.1:c.1504_1506delinsTGG	ENSP00000509861.1:p.Asn502Trp
ENST00000371953.8:c.985_987delinsTGG MANE Select	ENSP00000361021.3:p.Asn329Trp
ENST00000371953.7:c.985_987delinsTGG	ENSP00000361021.3:p.Asn329Trp
ENST00000472832.2:c.412_414delinsTGG	ENSP00000483066.1:p.Asn138Trp
NM_000314.5:c.985_987delinsTGG	NP_000305.3:p.Asn329Trp
NM_000314.6:c.985_987delinsTGG	NP_000305.3:p.Asn329Trp
NM_001304717.2:c.1504_1506delinsTGG	NP_001291646.2:p.Asn502Trp
NM_001304718.1:c.394_396delinsTGG	NP_001291647.1:p.Asn132Trp
XM_006717926.2:c.940_942delinsTGG	XP_006717989.1:p.Asn314Trp
XM_011539981.1:c.985_987delinsTGG	XP_011538283.1:p.Asn329Trp
XM_011539982.1:c.889_891delinsTGG	XP_011538284.1:p.Asn297Trp
XR_945791.1:n.1555_1557delinsTGG
NM_000314.7:c.985_987delinsTGG	NP_000305.3:p.Asn329Trp
NM_001304717.5:c.1504_1506delinsTGG	NP_001291646.4:p.Asn502Trp
NM_001304718.2:c.394_396delinsTGG	NP_001291647.1:p.Asn132Trp
NM_000314.8:c.985_987delinsTGG MANE Select	NP_000305.3:p.Asn329Trp