Canonical Allele Identifier: CA377487400

Gene: PTEN

Linked Data

• dbSNP Id: rs1860738514
• MyVariant Identifiers: chr10:g.89725183A>T (hg19) ; chr10:g.87965426A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965426A>T , CM000672.2:g.87965426A>T	GRCh38
NC_000010.10:g.89725183A>T , CM000672.1:g.89725183A>T	GRCh37
NC_000010.9:g.89715163A>T	NCBI36
NG_007466.2:g.106988A>T , LRG_311:g.106988A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1259A>T	ENSP00000514759.2:p.Asn420Ile
ENST00000710265.1:c.*195A>T	ENSP00000518161.1:n.*195A>T
ENST00000688158.2:n.1901A>T
ENST00000688922.2:c.*996A>T	ENSP00000508742.2:n.*996A>T
ENST00000700021.1:c.1121A>T	ENSP00000514757.1:p.Asn374Ile
ENST00000700022.1:c.*505A>T	ENSP00000514758.1:n.*505A>T
ENST00000700023.1:n.2324A>T
ENST00000700024.1:n.2558A>T
ENST00000706954.1:c.1166A>T	ENSP00000516674.1:p.Asn389Ile
ENST00000706955.1:c.*1201A>T	ENSP00000516675.1:n.*1201A>T
ENST00000686459.1:c.*752A>T	ENSP00000508909.1:n.*752A>T
ENST00000688158.1:c.*1277A>T	ENSP00000509254.1:n.*1277A>T
ENST00000688308.1:c.1166A>T	ENSP00000508752.1:p.Asn389Ile
ENST00000688922.1:c.1087A>T
ENST00000693560.1:c.1685A>T	ENSP00000509861.1:p.Asn562Ile
ENST00000371953.8:c.1166A>T MANE Select	ENSP00000361021.3:p.Asn389Ile
ENST00000371953.7:c.1166A>T	ENSP00000361021.3:p.Asn389Ile
NM_000314.5:c.1166A>T	NP_000305.3:p.Asn389Ile
NM_000314.6:c.1166A>T	NP_000305.3:p.Asn389Ile
NM_001304717.2:c.1685A>T	NP_001291646.2:p.Asn562Ile
NM_001304718.1:c.575A>T	NP_001291647.1:p.Asn192Ile
XM_006717926.2:c.1121A>T	XP_006717989.1:p.Asn374Ile
XM_011539982.1:c.1070A>T	XP_011538284.1:p.Asn357Ile
XR_945791.1:n.1736A>T
NM_000314.7:c.1166A>T	NP_000305.3:p.Asn389Ile
NM_001304717.5:c.1685A>T	NP_001291646.4:p.Asn562Ile
NM_001304718.2:c.575A>T	NP_001291647.1:p.Asn192Ile
NM_000314.8:c.1166A>T MANE Select	NP_000305.3:p.Asn389Ile