Canonical Allele Identifier: CA891834890

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894060_87894062delinsTCT , CM000672.2:g.87894060_87894062delinsTCT	GRCh38
NC_000010.10:g.89653817_89653819delinsTCT , CM000672.1:g.89653817_89653819delinsTCT	GRCh37
NC_000010.9:g.89643797_89643799delinsTCT	NCBI36
NG_007466.2:g.35622_35624delinsTCT , LRG_311:g.35622_35624delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.115_117delinsTCT	ENSP00000514759.2:p.Ala39Ser
ENST00000710265.1:c.115_117delinsTCT	ENSP00000518161.1:p.Ala39Ser
ENST00000472832.3:c.115_117delinsTCT	ENSP00000483066.2:p.Ala39Ser
ENST00000688158.2:n.899+13622_899+13624delinsTCT
ENST00000688922.2:c.115_117delinsTCT	ENSP00000508742.2:p.Ala39Ser
ENST00000700021.1:c.115_117delinsTCT	ENSP00000514757.1:p.Ala39Ser
ENST00000700022.1:c.115_117delinsTCT	ENSP00000514758.1:p.Ala39Ser
ENST00000706954.1:c.115_117delinsTCT	ENSP00000516674.1:p.Ala39Ser
ENST00000706955.1:c.*150_*152delinsTCT	ENSP00000516675.1:n.*150_*152delinsTCT
ENST00000686459.1:c.115_117delinsTCT	ENSP00000508909.1:p.Ala39Ser
ENST00000688158.1:c.*275+13622_*275+13624delinsTCT	ENSP00000509254.1:n.*275+13622_*275+13624delinsTCT
ENST00000688308.1:c.115_117delinsTCT	ENSP00000508752.1:p.Ala39Ser
ENST00000693560.1:c.634_636delinsTCT	ENSP00000509861.1:p.Ala212Ser
ENST00000371953.8:c.115_117delinsTCT MANE Select	ENSP00000361021.3:p.Ala39Ser
ENST00000371953.7:c.115_117delinsTCT	ENSP00000361021.3:p.Ala39Ser
ENST00000462694.1:n.117_119delinsTCT
ENST00000610634.1:c.13_15delinsTCT	ENSP00000477517.1:p.Ala5Ser
NM_000314.5:c.115_117delinsTCT	NP_000305.3:p.Ala39Ser
NM_000314.6:c.115_117delinsTCT	NP_000305.3:p.Ala39Ser
NM_001304717.2:c.634_636delinsTCT	NP_001291646.2:p.Ala212Ser
NM_001304718.1:c.-591_-589delinsTCT	NP_001291647.1:n.-591_-589delinsTCT
XM_006717926.2:c.115_117delinsTCT	XP_006717989.1:p.Ala39Ser
XM_011539981.1:c.115_117delinsTCT	XP_011538283.1:p.Ala39Ser
XM_011539982.1:c.68+13622_68+13624delinsTCT	XP_011538284.1:n.68+13622_68+13624delinsTCT
XR_945789.1:n.827_829delinsTCT
XR_945790.1:n.827_829delinsTCT
XR_945791.1:n.827_829delinsTCT
NM_000314.7:c.115_117delinsTCT	NP_000305.3:p.Ala39Ser
NM_001304717.5:c.634_636delinsTCT	NP_001291646.4:p.Ala212Ser
NM_001304718.2:c.-591_-589delinsTCT	NP_001291647.1:n.-591_-589delinsTCT
NM_000314.8:c.115_117delinsTCT MANE Select	NP_000305.3:p.Ala39Ser