Canonical Allele Identifier: CA1926189850

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960812_87960818delinsATTTTCT , CM000672.2:g.87960812_87960818delinsATTTTCT	GRCh38
NC_000010.10:g.89720569_89720575delinsATTTTCT , CM000672.1:g.89720569_89720575delinsATTTTCT	GRCh37
NC_000010.9:g.89710549_89710555delinsATTTTCT	NCBI36
NG_007466.2:g.102374_102380delinsATTTTCT , LRG_311:g.102374_102380delinsATTTTCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895-82_895-76delinsATTTTCT	ENSP00000514759.2:n.895-82_895-76delinsAT...
ENST00000710265.1:c.802-82_802-76delinsATTTTCT	ENSP00000518161.1:n.802-82_802-76delinsAT...
ENST00000472832.3:c.802-82_802-76delinsATTTTCT	ENSP00000483066.2:n.802-82_802-76delinsAT...
ENST00000688158.2:n.1537-82_1537-76delinsATTTTCT
ENST00000688922.2:c.*632-82_*632-76delinsATTTTCT	ENSP00000508742.2:n.*632-82_*632-76delins...
ENST00000700021.1:c.757-82_757-76delinsATTTTCT	ENSP00000514757.1:n.757-82_757-76delinsAT...
ENST00000700022.1:c.*141-82_*141-76delinsATTTTCT	ENSP00000514758.1:n.*141-82_*141-76delins...
ENST00000700023.1:n.1960-82_1960-76delinsATTTTCT
ENST00000700024.1:n.2194-82_2194-76delinsATTTTCT
ENST00000700025.1:n.1571-82_1571-76delinsATTTTCT
ENST00000700026.1:n.439-82_439-76delinsATTTTCT
ENST00000700029.1:c.729-82_729-76delinsATTTTCT
ENST00000706954.1:c.802-82_802-76delinsATTTTCT	ENSP00000516674.1:n.802-82_802-76delinsAT...
ENST00000706955.1:c.*837-82_*837-76delinsATTTTCT	ENSP00000516675.1:n.*837-82_*837-76delins...
ENST00000686459.1:c.*388-82_*388-76delinsATTTTCT	ENSP00000508909.1:n.*388-82_*388-76delins...
ENST00000688158.1:c.*913-82_*913-76delinsATTTTCT	ENSP00000509254.1:n.*913-82_*913-76delins...
ENST00000688308.1:c.802-82_802-76delinsATTTTCT	ENSP00000508752.1:n.802-82_802-76delinsAT...
ENST00000688922.1:c.723-82_723-76delinsATTTTCT
ENST00000693560.1:c.1321-82_1321-76delinsATTTTCT	ENSP00000509861.1:n.1321-82_1321-76delins...
ENST00000371953.8:c.802-82_802-76delinsATTTTCT MANE Select	ENSP00000361021.3:n.802-82_802-76delinsAT...
ENST00000371953.7:c.802-82_802-76delinsATTTTCT	ENSP00000361021.3:n.802-82_802-76delinsAT...
ENST00000472832.2:c.229-82_229-76delinsATTTTCT	ENSP00000483066.1:n.229-82_229-76delinsAT...
NM_000314.5:c.802-82_802-76delinsATTTTCT	NP_000305.3:n.802-82_802-76delinsATTTTCT
NM_000314.6:c.802-82_802-76delinsATTTTCT	NP_000305.3:n.802-82_802-76delinsATTTTCT
NM_001304717.2:c.1321-82_1321-76delinsATTTTCT	NP_001291646.2:n.1321-82_1321-76delinsATT...
NM_001304718.1:c.211-82_211-76delinsATTTTCT	NP_001291647.1:n.211-82_211-76delinsATTTT...
XM_006717926.2:c.757-82_757-76delinsATTTTCT	XP_006717989.1:n.757-82_757-76delinsATTTT...
XM_011539981.1:c.802-82_802-76delinsATTTTCT	XP_011538283.1:n.802-82_802-76delinsATTTT...
XM_011539982.1:c.706-82_706-76delinsATTTTCT	XP_011538284.1:n.706-82_706-76delinsATTTT...
XR_945791.1:n.1372-82_1372-76delinsATTTTCT
NM_000314.7:c.802-82_802-76delinsATTTTCT	NP_000305.3:n.802-82_802-76delinsATTTTCT
NM_001304717.5:c.1321-82_1321-76delinsATTTTCT	NP_001291646.4:n.1321-82_1321-76delinsATT...
NM_001304718.2:c.211-82_211-76delinsATTTTCT	NP_001291647.1:n.211-82_211-76delinsATTTT...
NM_000314.8:c.802-82_802-76delinsATTTTCT MANE Select	NP_000305.3:n.802-82_802-76delinsATTTTCT