Canonical Allele Identifier: CA1926189904

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960865_87960869delinsCTTTT , CM000672.2:g.87960865_87960869delinsCTTTT	GRCh38
NC_000010.10:g.89720622_89720626delinsCTTTT , CM000672.1:g.89720622_89720626delinsCTTTT	GRCh37
NC_000010.9:g.89710602_89710606delinsCTTTT	NCBI36
NG_007466.2:g.102427_102431delinsCTTTT , LRG_311:g.102427_102431delinsCTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.895-29_895-25delinsCTTTT	ENSP00000514759.2:n.895-29_895-25delinsCTTTT
ENST00000710265.1:c.802-29_802-25delinsCTTTT	ENSP00000518161.1:n.802-29_802-25delinsCTTTT
ENST00000472832.3:c.802-29_802-25delinsCTTTT	ENSP00000483066.2:n.802-29_802-25delinsCTTTT
ENST00000688158.2:n.1537-29_1537-25delinsCTTTT
ENST00000688922.2:c.*632-29_*632-25delinsCTTTT	ENSP00000508742.2:n.*632-29_*632-25delinsCTTTT
ENST00000700021.1:c.757-29_757-25delinsCTTTT	ENSP00000514757.1:n.757-29_757-25delinsCTTTT
ENST00000700022.1:c.*141-29_*141-25delinsCTTTT	ENSP00000514758.1:n.*141-29_*141-25delinsCTTTT
ENST00000700023.1:n.1960-29_1960-25delinsCTTTT
ENST00000700024.1:n.2194-29_2194-25delinsCTTTT
ENST00000700025.1:n.1571-29_1571-25delinsCTTTT
ENST00000700026.1:n.439-29_439-25delinsCTTTT
ENST00000700029.1:c.729-29_729-25delinsCTTTT
ENST00000706954.1:c.802-29_802-25delinsCTTTT	ENSP00000516674.1:n.802-29_802-25delinsCTTTT
ENST00000706955.1:c.*837-29_*837-25delinsCTTTT	ENSP00000516675.1:n.*837-29_*837-25delinsCTTTT
ENST00000686459.1:c.*388-29_*388-25delinsCTTTT	ENSP00000508909.1:n.*388-29_*388-25delinsCTTTT
ENST00000688158.1:c.*913-29_*913-25delinsCTTTT	ENSP00000509254.1:n.*913-29_*913-25delinsCTTTT
ENST00000688308.1:c.802-29_802-25delinsCTTTT	ENSP00000508752.1:n.802-29_802-25delinsCTTTT
ENST00000688922.1:c.723-29_723-25delinsCTTTT
ENST00000693560.1:c.1321-29_1321-25delinsCTTTT	ENSP00000509861.1:n.1321-29_1321-25delinsCTTTT
ENST00000371953.8:c.802-29_802-25delinsCTTTT MANE Select	ENSP00000361021.3:n.802-29_802-25delinsCTTTT
ENST00000371953.7:c.802-29_802-25delinsCTTTT	ENSP00000361021.3:n.802-29_802-25delinsCTTTT
ENST00000472832.2:c.229-29_229-25delinsCTTTT	ENSP00000483066.1:n.229-29_229-25delinsCTTTT
NM_000314.5:c.802-29_802-25delinsCTTTT	NP_000305.3:n.802-29_802-25delinsCTTTT
NM_000314.6:c.802-29_802-25delinsCTTTT	NP_000305.3:n.802-29_802-25delinsCTTTT
NM_001304717.2:c.1321-29_1321-25delinsCTTTT	NP_001291646.2:n.1321-29_1321-25delinsCTTTT
NM_001304718.1:c.211-29_211-25delinsCTTTT	NP_001291647.1:n.211-29_211-25delinsCTTTT
XM_006717926.2:c.757-29_757-25delinsCTTTT	XP_006717989.1:n.757-29_757-25delinsCTTTT
XM_011539981.1:c.802-29_802-25delinsCTTTT	XP_011538283.1:n.802-29_802-25delinsCTTTT
XM_011539982.1:c.706-29_706-25delinsCTTTT	XP_011538284.1:n.706-29_706-25delinsCTTTT
XR_945791.1:n.1372-29_1372-25delinsCTTTT
NM_000314.7:c.802-29_802-25delinsCTTTT	NP_000305.3:n.802-29_802-25delinsCTTTT
NM_001304717.5:c.1321-29_1321-25delinsCTTTT	NP_001291646.4:n.1321-29_1321-25delinsCTTTT
NM_001304718.2:c.211-29_211-25delinsCTTTT	NP_001291647.1:n.211-29_211-25delinsCTTTT
NM_000314.8:c.802-29_802-25delinsCTTTT MANE Select	NP_000305.3:n.802-29_802-25delinsCTTTT