Canonical Allele Identifier: CA16605991

Gene: PTEN

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957893T>C , CM000672.2:g.87957893T>C	GRCh38
NC_000010.10:g.89717650T>C , CM000672.1:g.89717650T>C	GRCh37
NC_000010.9:g.89707630T>C	NCBI36
NG_007466.2:g.99455T>C , LRG_311:g.99455T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.675T>C	ENSP00000514759.2:p.Tyr225=
ENST00000710265.1:c.675T>C	ENSP00000518161.1:p.Tyr225=
ENST00000472832.3:c.675T>C	ENSP00000483066.2:p.Tyr225=
ENST00000688158.2:n.1410T>C
ENST00000688922.2:c.*505T>C	ENSP00000508742.2:n.*505T>C
ENST00000700021.1:c.630T>C	ENSP00000514757.1:p.Tyr210=
ENST00000700022.1:c.*14T>C	ENSP00000514758.1:n.*14T>C
ENST00000700023.1:n.1833T>C
ENST00000700024.1:n.2067T>C
ENST00000700025.1:n.1444T>C
ENST00000700026.1:n.312T>C
ENST00000700029.1:c.509T>C
ENST00000706954.1:c.675T>C	ENSP00000516674.1:p.Tyr225=
ENST00000706955.1:c.*710T>C	ENSP00000516675.1:n.*710T>C
ENST00000686459.1:c.*261T>C	ENSP00000508909.1:n.*261T>C
ENST00000688158.1:c.*786T>C	ENSP00000509254.1:n.*786T>C
ENST00000688308.1:c.675T>C	ENSP00000508752.1:p.Tyr225=
ENST00000688922.1:c.596T>C
ENST00000693560.1:c.1194T>C	ENSP00000509861.1:p.Tyr398=
ENST00000371953.8:c.675T>C MANE Select	ENSP00000361021.3:p.Tyr225=
ENST00000371953.7:c.675T>C	ENSP00000361021.3:p.Tyr225=
ENST00000472832.2:c.102T>C	ENSP00000483066.1:p.Tyr34=
NM_000314.5:c.675T>C	NP_000305.3:p.Tyr225=
NM_000314.6:c.675T>C	NP_000305.3:p.Tyr225=
NM_001304717.2:c.1194T>C	NP_001291646.2:p.Tyr398=
NM_001304718.1:c.84T>C	NP_001291647.1:p.Tyr28=
XM_006717926.2:c.630T>C	XP_006717989.1:p.Tyr210=
XM_011539981.1:c.675T>C	XP_011538283.1:p.Tyr225=
XM_011539982.1:c.579T>C	XP_011538284.1:p.Tyr193=
XR_945791.1:n.1245T>C
NM_000314.7:c.675T>C	NP_000305.3:p.Tyr225=
NM_001304717.5:c.1194T>C	NP_001291646.4:p.Tyr398=
NM_001304718.2:c.84T>C	NP_001291647.1:p.Tyr28=
NM_000314.8:c.675T>C MANE Select	NP_000305.3:p.Tyr225=