Canonical Allele Identifier: CA1926188661

Gene: PTEN

Linked Data

• dbSNP Id: rs1860554172
• gnomAD v4: 10-87958076-ATATTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87958085_87958089del , CM000672.2:g.87958085_87958089del	GRCh38
NC_000010.10:g.89717842_89717846del , CM000672.1:g.89717842_89717846del	GRCh37
NC_000010.9:g.89707822_89707826del	NCBI36
NG_007466.2:g.99647_99651del , LRG_311:g.99647_99651del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.801+66_801+70del	ENSP00000514759.2:n.801+66_801+70del
ENST00000710265.1:c.801+66_801+70del	ENSP00000518161.1:n.801+66_801+70del
ENST00000472832.3:c.801+66_801+70del	ENSP00000483066.2:n.801+66_801+70del
ENST00000688158.2:n.1536+66_1536+70del
ENST00000688922.2:c.*631+66_*631+70del	ENSP00000508742.2:n.*631+66_*631+70del
ENST00000700021.1:c.756+66_756+70del	ENSP00000514757.1:n.756+66_756+70del
ENST00000700022.1:c.*140+66_*140+70del	ENSP00000514758.1:n.*140+66_*140+70del
ENST00000700023.1:n.1959+66_1959+70del
ENST00000700024.1:n.2193+66_2193+70del
ENST00000700025.1:n.1570+66_1570+70del
ENST00000700026.1:n.438+66_438+70del
ENST00000700029.1:c.635+66_635+70del
ENST00000706954.1:c.801+66_801+70del	ENSP00000516674.1:n.801+66_801+70del
ENST00000706955.1:c.*836+66_*836+70del	ENSP00000516675.1:n.*836+66_*836+70del
ENST00000686459.1:c.*387+66_*387+70del	ENSP00000508909.1:n.*387+66_*387+70del
ENST00000688158.1:c.*912+66_*912+70del	ENSP00000509254.1:n.*912+66_*912+70del
ENST00000688308.1:c.801+66_801+70del	ENSP00000508752.1:n.801+66_801+70del
ENST00000688922.1:c.722+66_722+70del
ENST00000693560.1:c.1320+66_1320+70del	ENSP00000509861.1:n.1320+66_1320+70del
ENST00000371953.8:c.801+66_801+70del MANE Select	ENSP00000361021.3:n.801+66_801+70del
ENST00000371953.7:c.801+66_801+70del	ENSP00000361021.3:n.801+66_801+70del
ENST00000472832.2:c.228+66_228+70del	ENSP00000483066.1:n.228+66_228+70del
NM_000314.5:c.801+66_801+70del	NP_000305.3:n.801+66_801+70del
NM_000314.6:c.801+66_801+70del	NP_000305.3:n.801+66_801+70del
NM_001304717.2:c.1320+66_1320+70del	NP_001291646.2:n.1320+66_1320+70del
NM_001304718.1:c.210+66_210+70del	NP_001291647.1:n.210+66_210+70del
XM_006717926.2:c.756+66_756+70del	XP_006717989.1:n.756+66_756+70del
XM_011539981.1:c.801+66_801+70del	XP_011538283.1:n.801+66_801+70del
XM_011539982.1:c.705+66_705+70del	XP_011538284.1:n.705+66_705+70del
XR_945791.1:n.1371+66_1371+70del
NM_000314.7:c.801+66_801+70del	NP_000305.3:n.801+66_801+70del
NM_001304717.5:c.1320+66_1320+70del	NP_001291646.4:n.1320+66_1320+70del
NM_001304718.2:c.210+66_210+70del	NP_001291647.1:n.210+66_210+70del
NM_000314.8:c.801+66_801+70del MANE Select	NP_000305.3:n.801+66_801+70del