Canonical Allele Identifier: CA1926188627
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958017_87958019delinsAAG , CM000672.2:g.87958017_87958019delinsAAG GRCh38
NC_000010.10:g.89717774_89717776delinsAAG , CM000672.1:g.89717774_89717776delinsAAG GRCh37
NC_000010.9:g.89707754_89707756delinsAAG NCBI36
NG_007466.2:g.99579_99581delinsAAG , LRG_311:g.99579_99581delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.799_801delinsAAG ENSP00000514759.2:p.Lys267=
ENST00000710265.1:c.799_801delinsAAG ENSP00000518161.1:p.Lys267=
ENST00000472832.3:c.799_801delinsAAG ENSP00000483066.2:p.Lys267=
ENST00000688158.2:n.1534_1536delinsAAG
ENST00000688922.2:c.*629_*631delinsAAG ENSP00000508742.2:n.*629_*631delinsAAG
ENST00000700021.1:c.754_756delinsAAG ENSP00000514757.1:p.Lys252=
ENST00000700022.1:c.*138_*140delinsAAG ENSP00000514758.1:n.*138_*140delinsAAG
ENST00000700023.1:n.1957_1959delinsAAG
ENST00000700024.1:n.2191_2193delinsAAG
ENST00000700025.1:n.1568_1570delinsAAG
ENST00000700026.1:n.436_438delinsAAG
ENST00000700029.1:c.633_635delinsAAG
ENST00000706954.1:c.799_801delinsAAG ENSP00000516674.1:p.Lys267=
ENST00000706955.1:c.*834_*836delinsAAG ENSP00000516675.1:n.*834_*836delinsAAG
ENST00000686459.1:c.*385_*387delinsAAG ENSP00000508909.1:n.*385_*387delinsAAG
ENST00000688158.1:c.*910_*912delinsAAG ENSP00000509254.1:n.*910_*912delinsAAG
ENST00000688308.1:c.799_801delinsAAG ENSP00000508752.1:p.Lys267=
ENST00000688922.1:c.720_722delinsAAG
ENST00000693560.1:c.1318_1320delinsAAG ENSP00000509861.1:p.Lys440=
ENST00000371953.8:c.799_801delinsAAG MANE Select ENSP00000361021.3:p.Lys267=
ENST00000371953.7:c.799_801delinsAAG ENSP00000361021.3:p.Lys267=
ENST00000472832.2:c.226_228delinsAAG ENSP00000483066.1:p.Lys76=
NM_000314.5:c.799_801delinsAAG NP_000305.3:p.Lys267=
NM_000314.6:c.799_801delinsAAG NP_000305.3:p.Lys267=
NM_001304717.2:c.1318_1320delinsAAG NP_001291646.2:p.Lys440=
NM_001304718.1:c.208_210delinsAAG NP_001291647.1:p.Lys70=
XM_006717926.2:c.754_756delinsAAG XP_006717989.1:p.Lys252=
XM_011539981.1:c.799_801delinsAAG XP_011538283.1:p.Lys267=
XM_011539982.1:c.703_705delinsAAG XP_011538284.1:p.Lys235=
XR_945791.1:n.1369_1371delinsAAG
NM_000314.7:c.799_801delinsAAG NP_000305.3:p.Lys267=
NM_001304717.5:c.1318_1320delinsAAG NP_001291646.4:p.Lys440=
NM_001304718.2:c.208_210delinsAAG NP_001291647.1:p.Lys70=
NM_000314.8:c.799_801delinsAAG MANE Select NP_000305.3:p.Lys267=