Canonical Allele Identifier: CA1926173999

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965415T= , CM000672.2:g.87965415T=	GRCh38
NC_000010.10:g.89725172T= , CM000672.1:g.89725172T=	GRCh37
NC_000010.9:g.89715152T=	NCBI36
NG_007466.2:g.106977T= , LRG_311:g.106977T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1248T=	ENSP00000514759.2:p.Ser416=
ENST00000710265.1:c.*184T=	ENSP00000518161.1:n.*184T=
ENST00000688158.2:n.1890T=
ENST00000688922.2:c.*985T=	ENSP00000508742.2:n.*985T=
ENST00000700021.1:c.1110T=	ENSP00000514757.1:p.Ser370=
ENST00000700022.1:c.*494T=	ENSP00000514758.1:n.*494T=
ENST00000700023.1:n.2313T=
ENST00000700024.1:n.2547T=
ENST00000706954.1:c.1155T=	ENSP00000516674.1:p.Ser385=
ENST00000706955.1:c.*1190T=	ENSP00000516675.1:n.*1190T=
ENST00000686459.1:c.*741T=	ENSP00000508909.1:n.*741T=
ENST00000688158.1:c.*1266T=	ENSP00000509254.1:n.*1266T=
ENST00000688308.1:c.1155T=	ENSP00000508752.1:p.Ser385=
ENST00000688922.1:c.1076T=
ENST00000693560.1:c.1674T=	ENSP00000509861.1:p.Ser558=
ENST00000371953.8:c.1155T= MANE Select	ENSP00000361021.3:p.Ser385=
ENST00000371953.7:c.1155T=	ENSP00000361021.3:p.Ser385=
NM_000314.5:c.1155T=	NP_000305.3:p.Ser385=
NM_000314.6:c.1155T=	NP_000305.3:p.Ser385=
NM_001304717.2:c.1674T=	NP_001291646.2:p.Ser558=
NM_001304718.1:c.564T=	NP_001291647.1:p.Ser188=
XM_006717926.2:c.1110T=	XP_006717989.1:p.Ser370=
XM_011539982.1:c.1059T=	XP_011538284.1:p.Ser353=
XR_945791.1:n.1725T=
NM_000314.7:c.1155T=	NP_000305.3:p.Ser385=
NM_001304717.5:c.1674T=	NP_001291646.4:p.Ser558=
NM_001304718.2:c.564T=	NP_001291647.1:p.Ser188=
NM_000314.8:c.1155T= MANE Select	NP_000305.3:p.Ser385=