Canonical Allele Identifier: CA891836033

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961009_87961010delinsAT , CM000672.2:g.87961009_87961010delinsAT	GRCh38
NC_000010.10:g.89720766_89720767delinsAT , CM000672.1:g.89720766_89720767delinsAT	GRCh37
NC_000010.9:g.89710746_89710747delinsAT	NCBI36
NG_007466.2:g.102571_102572delinsAT , LRG_311:g.102571_102572delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1010_1011delinsAT	ENSP00000514759.2:p.Ile337Asn
ENST00000710265.1:c.917_918delinsAT	ENSP00000518161.1:p.Ile306Asn
ENST00000472832.3:c.917_918delinsAT	ENSP00000483066.2:p.Ile306Asn
ENST00000688158.2:n.1652_1653delinsAT
ENST00000688922.2:c.*747_*748delinsAT	ENSP00000508742.2:n.*747_*748delinsAT
ENST00000700021.1:c.872_873delinsAT	ENSP00000514757.1:p.Ile291Asn
ENST00000700022.1:c.*256_*257delinsAT	ENSP00000514758.1:n.*256_*257delinsAT
ENST00000700023.1:n.2075_2076delinsAT
ENST00000700024.1:n.2309_2310delinsAT
ENST00000700025.1:n.1686_1687delinsAT
ENST00000700026.1:n.554_555delinsAT
ENST00000706954.1:c.917_918delinsAT	ENSP00000516674.1:p.Ile306Asn
ENST00000706955.1:c.*952_*953delinsAT	ENSP00000516675.1:n.*952_*953delinsAT
ENST00000686459.1:c.*503_*504delinsAT	ENSP00000508909.1:n.*503_*504delinsAT
ENST00000688158.1:c.*1028_*1029delinsAT	ENSP00000509254.1:n.*1028_*1029delinsAT
ENST00000688308.1:c.917_918delinsAT	ENSP00000508752.1:p.Ile306Asn
ENST00000688922.1:c.838_839delinsAT
ENST00000693560.1:c.1436_1437delinsAT	ENSP00000509861.1:p.Ile479Asn
ENST00000371953.8:c.917_918delinsAT MANE Select	ENSP00000361021.3:p.Ile306Asn
ENST00000371953.7:c.917_918delinsAT	ENSP00000361021.3:p.Ile306Asn
ENST00000472832.2:c.344_345delinsAT	ENSP00000483066.1:p.Ile115Asn
NM_000314.5:c.917_918delinsAT	NP_000305.3:p.Ile306Asn
NM_000314.6:c.917_918delinsAT	NP_000305.3:p.Ile306Asn
NM_001304717.2:c.1436_1437delinsAT	NP_001291646.2:p.Ile479Asn
NM_001304718.1:c.326_327delinsAT	NP_001291647.1:p.Ile109Asn
XM_006717926.2:c.872_873delinsAT	XP_006717989.1:p.Ile291Asn
XM_011539981.1:c.917_918delinsAT	XP_011538283.1:p.Ile306Asn
XM_011539982.1:c.821_822delinsAT	XP_011538284.1:p.Ile274Asn
XR_945791.1:n.1487_1488delinsAT
NM_000314.7:c.917_918delinsAT	NP_000305.3:p.Ile306Asn
NM_001304717.5:c.1436_1437delinsAT	NP_001291646.4:p.Ile479Asn
NM_001304718.2:c.326_327delinsAT	NP_001291647.1:p.Ile109Asn
NM_000314.8:c.917_918delinsAT MANE Select	NP_000305.3:p.Ile306Asn