Canonical Allele Identifier: CA377487364

Gene: PTEN

Linked Data

• dbSNP Id: rs2132290063
• MyVariant Identifiers: chr10:g.89725168A>T (hg19) ; chr10:g.87965411A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965411A>T , CM000672.2:g.87965411A>T	GRCh38
NC_000010.10:g.89725168A>T , CM000672.1:g.89725168A>T	GRCh37
NC_000010.9:g.89715148A>T	NCBI36
NG_007466.2:g.106973A>T , LRG_311:g.106973A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1244A>T	ENSP00000514759.2:p.Asp415Val
ENST00000710265.1:c.*180A>T	ENSP00000518161.1:n.*180A>T
ENST00000688158.2:n.1886A>T
ENST00000688922.2:c.*981A>T	ENSP00000508742.2:n.*981A>T
ENST00000700021.1:c.1106A>T	ENSP00000514757.1:p.Asp369Val
ENST00000700022.1:c.*490A>T	ENSP00000514758.1:n.*490A>T
ENST00000700023.1:n.2309A>T
ENST00000700024.1:n.2543A>T
ENST00000706954.1:c.1151A>T	ENSP00000516674.1:p.Asp384Val
ENST00000706955.1:c.*1186A>T	ENSP00000516675.1:n.*1186A>T
ENST00000686459.1:c.*737A>T	ENSP00000508909.1:n.*737A>T
ENST00000688158.1:c.*1262A>T	ENSP00000509254.1:n.*1262A>T
ENST00000688308.1:c.1151A>T	ENSP00000508752.1:p.Asp384Val
ENST00000688922.1:c.1072A>T
ENST00000693560.1:c.1670A>T	ENSP00000509861.1:p.Asp557Val
ENST00000371953.8:c.1151A>T MANE Select	ENSP00000361021.3:p.Asp384Val
ENST00000371953.7:c.1151A>T	ENSP00000361021.3:p.Asp384Val
NM_000314.5:c.1151A>T	NP_000305.3:p.Asp384Val
NM_000314.6:c.1151A>T	NP_000305.3:p.Asp384Val
NM_001304717.2:c.1670A>T	NP_001291646.2:p.Asp557Val
NM_001304718.1:c.560A>T	NP_001291647.1:p.Asp187Val
XM_006717926.2:c.1106A>T	XP_006717989.1:p.Asp369Val
XM_011539982.1:c.1055A>T	XP_011538284.1:p.Asp352Val
XR_945791.1:n.1721A>T
NM_000314.7:c.1151A>T	NP_000305.3:p.Asp384Val
NM_001304717.5:c.1670A>T	NP_001291646.4:p.Asp557Val
NM_001304718.2:c.560A>T	NP_001291647.1:p.Asp187Val
NM_000314.8:c.1151A>T MANE Select	NP_000305.3:p.Asp384Val