Canonical Allele Identifier: CA930923740

Gene: PTEN

Linked Data

• dbSNP Id: rs1860608523
• gnomAD v3: 10-87960723-TATA-T
• gnomAD v4: 10-87960723-TATA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960727_87960729del , CM000672.2:g.87960727_87960729del	GRCh38
NC_000010.10:g.89720484_89720486del , CM000672.1:g.89720484_89720486del	GRCh37
NC_000010.9:g.89710464_89710466del	NCBI36
NG_007466.2:g.102289_102291del , LRG_311:g.102289_102291del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.895-167_895-165del	ENSP00000514759.2:n.895-167_895-165del
ENST00000710265.1:c.802-167_802-165del	ENSP00000518161.1:n.802-167_802-165del
ENST00000472832.3:c.802-167_802-165del	ENSP00000483066.2:n.802-167_802-165del
ENST00000688158.2:n.1537-167_1537-165del
ENST00000688922.2:c.*632-167_*632-165del	ENSP00000508742.2:n.*632-167_*632-165del
ENST00000700021.1:c.757-167_757-165del	ENSP00000514757.1:n.757-167_757-165del
ENST00000700022.1:c.*141-167_*141-165del	ENSP00000514758.1:n.*141-167_*141-165del
ENST00000700023.1:n.1960-167_1960-165del
ENST00000700024.1:n.2194-167_2194-165del
ENST00000700025.1:n.1571-167_1571-165del
ENST00000700026.1:n.439-167_439-165del
ENST00000700029.1:c.729-167_729-165del
ENST00000706954.1:c.802-167_802-165del	ENSP00000516674.1:n.802-167_802-165del
ENST00000706955.1:c.*837-167_*837-165del	ENSP00000516675.1:n.*837-167_*837-165del
ENST00000686459.1:c.*388-167_*388-165del	ENSP00000508909.1:n.*388-167_*388-165del
ENST00000688158.1:c.*913-167_*913-165del	ENSP00000509254.1:n.*913-167_*913-165del
ENST00000688308.1:c.802-167_802-165del	ENSP00000508752.1:n.802-167_802-165del
ENST00000688922.1:c.723-167_723-165del
ENST00000693560.1:c.1321-167_1321-165del	ENSP00000509861.1:n.1321-167_1321-165del
ENST00000371953.8:c.802-167_802-165del MANE Select	ENSP00000361021.3:n.802-167_802-165del
ENST00000371953.7:c.802-167_802-165del	ENSP00000361021.3:n.802-167_802-165del
ENST00000472832.2:c.229-167_229-165del	ENSP00000483066.1:n.229-167_229-165del
NM_000314.5:c.802-167_802-165del	NP_000305.3:n.802-167_802-165del
NM_000314.6:c.802-167_802-165del	NP_000305.3:n.802-167_802-165del
NM_001304717.2:c.1321-167_1321-165del	NP_001291646.2:n.1321-167_1321-165del
NM_001304718.1:c.211-167_211-165del	NP_001291647.1:n.211-167_211-165del
XM_006717926.2:c.757-167_757-165del	XP_006717989.1:n.757-167_757-165del
XM_011539981.1:c.802-167_802-165del	XP_011538283.1:n.802-167_802-165del
XM_011539982.1:c.706-167_706-165del	XP_011538284.1:n.706-167_706-165del
XR_945791.1:n.1372-167_1372-165del
NM_000314.7:c.802-167_802-165del	NP_000305.3:n.802-167_802-165del
NM_001304717.5:c.1321-167_1321-165del	NP_001291646.4:n.1321-167_1321-165del
NM_001304718.2:c.211-167_211-165del	NP_001291647.1:n.211-167_211-165del
NM_000314.8:c.802-167_802-165del MANE Select	NP_000305.3:n.802-167_802-165del