Canonical Allele Identifier: CA669552833

Gene: PTEN

Linked Data

• dbSNP Id: rs1488569786
• gnomAD v3: 10-87957778-TAA-T
• gnomAD v4: 10-87957778-TAA-T
• MyVariant Identifiers: chr10:g.87957779_87957780del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957781_87957782del , CM000672.2:g.87957781_87957782del	GRCh38
NC_000010.10:g.89717538_89717539del , CM000672.1:g.89717538_89717539del	GRCh37
NC_000010.9:g.89707518_89707519del	NCBI36
NG_007466.2:g.99343_99344del , LRG_311:g.99343_99344del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.635-72_635-71del	ENSP00000514759.2:n.635-72_635-71del
ENST00000710265.1:c.635-72_635-71del	ENSP00000518161.1:n.635-72_635-71del
ENST00000472832.3:c.635-72_635-71del	ENSP00000483066.2:n.635-72_635-71del
ENST00000688158.2:n.1370-72_1370-71del
ENST00000688922.2:c.*465-72_*465-71del	ENSP00000508742.2:n.*465-72_*465-71del
ENST00000700021.1:c.590-72_590-71del	ENSP00000514757.1:n.590-72_590-71del
ENST00000700022.1:c.493-72_493-71del	ENSP00000514758.1:n.493-72_493-71del
ENST00000700023.1:n.1793-72_1793-71del
ENST00000700024.1:n.2027-72_2027-71del
ENST00000700025.1:n.1404-72_1404-71del
ENST00000700026.1:n.200_201del
ENST00000700029.1:c.469-72_469-71del
ENST00000706954.1:c.635-72_635-71del	ENSP00000516674.1:n.635-72_635-71del
ENST00000706955.1:c.*670-72_*670-71del	ENSP00000516675.1:n.*670-72_*670-71del
ENST00000686459.1:c.*221-72_*221-71del	ENSP00000508909.1:n.*221-72_*221-71del
ENST00000688158.1:c.*746-72_*746-71del	ENSP00000509254.1:n.*746-72_*746-71del
ENST00000688308.1:c.635-72_635-71del	ENSP00000508752.1:n.635-72_635-71del
ENST00000688922.1:c.556-72_556-71del
ENST00000693560.1:c.1154-72_1154-71del	ENSP00000509861.1:n.1154-72_1154-71del
ENST00000371953.8:c.635-72_635-71del MANE Select	ENSP00000361021.3:n.635-72_635-71del
ENST00000371953.7:c.635-72_635-71del	ENSP00000361021.3:n.635-72_635-71del
ENST00000472832.2:c.62-72_62-71del	ENSP00000483066.1:n.62-72_62-71del
NM_000314.5:c.635-72_635-71del	NP_000305.3:n.635-72_635-71del
NM_000314.6:c.635-72_635-71del	NP_000305.3:n.635-72_635-71del
NM_001304717.2:c.1154-72_1154-71del	NP_001291646.2:n.1154-72_1154-71del
NM_001304718.1:c.44-72_44-71del	NP_001291647.1:n.44-72_44-71del
XM_006717926.2:c.590-72_590-71del	XP_006717989.1:n.590-72_590-71del
XM_011539981.1:c.635-72_635-71del	XP_011538283.1:n.635-72_635-71del
XM_011539982.1:c.539-72_539-71del	XP_011538284.1:n.539-72_539-71del
XR_945791.1:n.1205-72_1205-71del
NM_000314.7:c.635-72_635-71del	NP_000305.3:n.635-72_635-71del
NM_001304717.5:c.1154-72_1154-71del	NP_001291646.4:n.1154-72_1154-71del
NM_001304718.2:c.44-72_44-71del	NP_001291647.1:n.44-72_44-71del
NM_000314.8:c.635-72_635-71del MANE Select	NP_000305.3:n.635-72_635-71del