Canonical Allele Identifier: CA891834879

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894060_87894061delinsCA , CM000672.2:g.87894060_87894061delinsCA	GRCh38
NC_000010.10:g.89653817_89653818delinsCA , CM000672.1:g.89653817_89653818delinsCA	GRCh37
NC_000010.9:g.89643797_89643798delinsCA	NCBI36
NG_007466.2:g.35622_35623delinsCA , LRG_311:g.35622_35623delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.115_116delinsCA	ENSP00000514759.2:p.Ala39Gln
ENST00000710265.1:c.115_116delinsCA	ENSP00000518161.1:p.Ala39Gln
ENST00000472832.3:c.115_116delinsCA	ENSP00000483066.2:p.Ala39Gln
ENST00000688158.2:n.899+13622_899+13623delinsCA
ENST00000688922.2:c.115_116delinsCA	ENSP00000508742.2:p.Ala39Gln
ENST00000700021.1:c.115_116delinsCA	ENSP00000514757.1:p.Ala39Gln
ENST00000700022.1:c.115_116delinsCA	ENSP00000514758.1:p.Ala39Gln
ENST00000706954.1:c.115_116delinsCA	ENSP00000516674.1:p.Ala39Gln
ENST00000706955.1:c.*150_*151delinsCA	ENSP00000516675.1:n.*150_*151delinsCA
ENST00000686459.1:c.115_116delinsCA	ENSP00000508909.1:p.Ala39Gln
ENST00000688158.1:c.*275+13622_*275+13623delinsCA	ENSP00000509254.1:n.*275+13622_*275+13623delinsCA
ENST00000688308.1:c.115_116delinsCA	ENSP00000508752.1:p.Ala39Gln
ENST00000693560.1:c.634_635delinsCA	ENSP00000509861.1:p.Ala212Gln
ENST00000371953.8:c.115_116delinsCA MANE Select	ENSP00000361021.3:p.Ala39Gln
ENST00000371953.7:c.115_116delinsCA	ENSP00000361021.3:p.Ala39Gln
ENST00000462694.1:n.117_118delinsCA
ENST00000610634.1:c.13_14delinsCA	ENSP00000477517.1:p.Ala5Gln
NM_000314.5:c.115_116delinsCA	NP_000305.3:p.Ala39Gln
NM_000314.6:c.115_116delinsCA	NP_000305.3:p.Ala39Gln
NM_001304717.2:c.634_635delinsCA	NP_001291646.2:p.Ala212Gln
NM_001304718.1:c.-591_-590delinsCA	NP_001291647.1:n.-591_-590delinsCA
XM_006717926.2:c.115_116delinsCA	XP_006717989.1:p.Ala39Gln
XM_011539981.1:c.115_116delinsCA	XP_011538283.1:p.Ala39Gln
XM_011539982.1:c.68+13622_68+13623delinsCA	XP_011538284.1:n.68+13622_68+13623delinsCA
XR_945789.1:n.827_828delinsCA
XR_945790.1:n.827_828delinsCA
XR_945791.1:n.827_828delinsCA
NM_000314.7:c.115_116delinsCA	NP_000305.3:p.Ala39Gln
NM_001304717.5:c.634_635delinsCA	NP_001291646.4:p.Ala212Gln
NM_001304718.2:c.-591_-590delinsCA	NP_001291647.1:n.-591_-590delinsCA
NM_000314.8:c.115_116delinsCA MANE Select	NP_000305.3:p.Ala39Gln