Canonical Allele Identifier: CA2722437213

Gene: PTEN

Linked Data

• dbSNP Id: rs2132281074

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960703_87960705dup , CM000672.2:g.87960703_87960705dup	GRCh38
NC_000010.10:g.89720460_89720462dup , CM000672.1:g.89720460_89720462dup	GRCh37
NC_000010.9:g.89710440_89710442dup	NCBI36
NG_007466.2:g.102265_102267dup , LRG_311:g.102265_102267dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895-191_895-189dup	ENSP00000514759.2:n.895-191_895-189dup
ENST00000710265.1:c.802-191_802-189dup	ENSP00000518161.1:n.802-191_802-189dup
ENST00000472832.3:c.802-191_802-189dup	ENSP00000483066.2:n.802-191_802-189dup
ENST00000688158.2:n.1537-191_1537-189dup
ENST00000688922.2:c.*632-191_*632-189dup	ENSP00000508742.2:n.*632-191_*632-189dup
ENST00000700021.1:c.757-191_757-189dup	ENSP00000514757.1:n.757-191_757-189dup
ENST00000700022.1:c.*141-191_*141-189dup	ENSP00000514758.1:n.*141-191_*141-189dup
ENST00000700023.1:n.1960-191_1960-189dup
ENST00000700024.1:n.2194-191_2194-189dup
ENST00000700025.1:n.1571-191_1571-189dup
ENST00000700026.1:n.439-191_439-189dup
ENST00000700029.1:c.729-191_729-189dup
ENST00000706954.1:c.802-191_802-189dup	ENSP00000516674.1:n.802-191_802-189dup
ENST00000706955.1:c.*837-191_*837-189dup	ENSP00000516675.1:n.*837-191_*837-189dup
ENST00000686459.1:c.*388-191_*388-189dup	ENSP00000508909.1:n.*388-191_*388-189dup
ENST00000688158.1:c.*913-191_*913-189dup	ENSP00000509254.1:n.*913-191_*913-189dup
ENST00000688308.1:c.802-191_802-189dup	ENSP00000508752.1:n.802-191_802-189dup
ENST00000688922.1:c.723-191_723-189dup
ENST00000693560.1:c.1321-191_1321-189dup	ENSP00000509861.1:n.1321-191_1321-189dup
ENST00000371953.8:c.802-191_802-189dup MANE Select	ENSP00000361021.3:n.802-191_802-189dup
ENST00000371953.7:c.802-191_802-189dup	ENSP00000361021.3:n.802-191_802-189dup
ENST00000472832.2:c.229-191_229-189dup	ENSP00000483066.1:n.229-191_229-189dup
NM_000314.5:c.802-191_802-189dup	NP_000305.3:n.802-191_802-189dup
NM_000314.6:c.802-191_802-189dup	NP_000305.3:n.802-191_802-189dup
NM_001304717.2:c.1321-191_1321-189dup	NP_001291646.2:n.1321-191_1321-189dup
NM_001304718.1:c.211-191_211-189dup	NP_001291647.1:n.211-191_211-189dup
XM_006717926.2:c.757-191_757-189dup	XP_006717989.1:n.757-191_757-189dup
XM_011539981.1:c.802-191_802-189dup	XP_011538283.1:n.802-191_802-189dup
XM_011539982.1:c.706-191_706-189dup	XP_011538284.1:n.706-191_706-189dup
XR_945791.1:n.1372-191_1372-189dup
NM_000314.7:c.802-191_802-189dup	NP_000305.3:n.802-191_802-189dup
NM_001304717.5:c.1321-191_1321-189dup	NP_001291646.4:n.1321-191_1321-189dup
NM_001304718.2:c.211-191_211-189dup	NP_001291647.1:n.211-191_211-189dup
NM_000314.8:c.802-191_802-189dup MANE Select	NP_000305.3:n.802-191_802-189dup