Canonical Allele Identifier: CA377485777

Gene: PTEN

Linked Data

• dbSNP Id: rs2132282518
• MyVariant Identifiers: chr10:g.89720748T>A (hg19) ; chr10:g.87960991T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960991T>A , CM000672.2:g.87960991T>A	GRCh38
NC_000010.10:g.89720748T>A , CM000672.1:g.89720748T>A	GRCh37
NC_000010.9:g.89710728T>A	NCBI36
NG_007466.2:g.102553T>A , LRG_311:g.102553T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.992T>A	ENSP00000514759.2:p.Ile331Asn
ENST00000710265.1:c.899T>A	ENSP00000518161.1:p.Ile300Asn
ENST00000472832.3:c.899T>A	ENSP00000483066.2:p.Ile300Asn
ENST00000688158.2:n.1634T>A
ENST00000688922.2:c.*729T>A	ENSP00000508742.2:n.*729T>A
ENST00000700021.1:c.854T>A	ENSP00000514757.1:p.Ile285Asn
ENST00000700022.1:c.*238T>A	ENSP00000514758.1:n.*238T>A
ENST00000700023.1:n.2057T>A
ENST00000700024.1:n.2291T>A
ENST00000700025.1:n.1668T>A
ENST00000700026.1:n.536T>A
ENST00000706954.1:c.899T>A	ENSP00000516674.1:p.Ile300Asn
ENST00000706955.1:c.*934T>A	ENSP00000516675.1:n.*934T>A
ENST00000686459.1:c.*485T>A	ENSP00000508909.1:n.*485T>A
ENST00000688158.1:c.*1010T>A	ENSP00000509254.1:n.*1010T>A
ENST00000688308.1:c.899T>A	ENSP00000508752.1:p.Ile300Asn
ENST00000688922.1:c.820T>A
ENST00000693560.1:c.1418T>A	ENSP00000509861.1:p.Ile473Asn
ENST00000371953.8:c.899T>A MANE Select	ENSP00000361021.3:p.Ile300Asn
ENST00000371953.7:c.899T>A	ENSP00000361021.3:p.Ile300Asn
ENST00000472832.2:c.326T>A	ENSP00000483066.1:p.Ile109Asn
NM_000314.5:c.899T>A	NP_000305.3:p.Ile300Asn
NM_000314.6:c.899T>A	NP_000305.3:p.Ile300Asn
NM_001304717.2:c.1418T>A	NP_001291646.2:p.Ile473Asn
NM_001304718.1:c.308T>A	NP_001291647.1:p.Ile103Asn
XM_006717926.2:c.854T>A	XP_006717989.1:p.Ile285Asn
XM_011539981.1:c.899T>A	XP_011538283.1:p.Ile300Asn
XM_011539982.1:c.803T>A	XP_011538284.1:p.Ile268Asn
XR_945791.1:n.1469T>A
NM_000314.7:c.899T>A	NP_000305.3:p.Ile300Asn
NM_001304717.5:c.1418T>A	NP_001291646.4:p.Ile473Asn
NM_001304718.2:c.308T>A	NP_001291647.1:p.Ile103Asn
NM_000314.8:c.899T>A MANE Select	NP_000305.3:p.Ile300Asn