Canonical Allele Identifier: CA669574161

Gene: PTEN

Linked Data

• dbSNP Id: rs1381756660
• MyVariant Identifiers: chr10:g.87966775C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966775C>T , CM000672.2:g.87966775C>T	GRCh38
NC_000010.10:g.89726532C>T , CM000672.1:g.89726532C>T	GRCh37
NC_000010.9:g.89716512C>T	NCBI36
NG_007466.2:g.108337C>T , LRG_311:g.108337C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*1303C>T	ENSP00000514759.2:n.*1303C>T
ENST00000710265.1:c.*1544C>T	ENSP00000518161.1:n.*1544C>T
ENST00000688158.2:n.3250C>T
ENST00000688922.2:c.*2345C>T	ENSP00000508742.2:n.*2345C>T
ENST00000700021.1:c.*1303C>T	ENSP00000514757.1:n.*1303C>T
ENST00000700022.1:c.*1854C>T	ENSP00000514758.1:n.*1854C>T
ENST00000700024.1:n.3907C>T
ENST00000706954.1:c.*1303C>T	ENSP00000516674.1:n.*1303C>T
ENST00000706955.1:c.*2550C>T	ENSP00000516675.1:n.*2550C>T
ENST00000688158.1:c.*2626C>T	ENSP00000509254.1:n.*2626C>T
ENST00000688308.1:c.*1303C>T	ENSP00000508752.1:n.*1303C>T
ENST00000688922.1:c.2436C>T
ENST00000693560.1:c.*1303C>T	ENSP00000509861.1:n.*1303C>T
ENST00000371953.8:c.*1303C>T MANE Select	ENSP00000361021.3:n.*1303C>T
ENST00000371953.7:c.*1303C>T	ENSP00000361021.3:n.*1303C>T
NM_000314.5:c.*1303C>T	NP_000305.3:n.*1303C>T
NM_000314.6:c.*1303C>T	NP_000305.3:n.*1303C>T
NM_001304717.2:c.*1303C>T	NP_001291646.2:n.*1303C>T
NM_001304718.1:c.*1303C>T	NP_001291647.1:n.*1303C>T
XM_006717926.2:c.*1303C>T	XP_006717989.1:n.*1303C>T
XM_011539982.1:c.*1303C>T	XP_011538284.1:n.*1303C>T
XR_945791.1:n.3085C>T
NM_000314.7:c.*1303C>T	NP_000305.3:n.*1303C>T
NM_001304717.5:c.*1303C>T	NP_001291646.4:n.*1303C>T
NM_001304718.2:c.*1303C>T	NP_001291647.1:n.*1303C>T
NM_000314.8:c.*1303C>T MANE Select	NP_000305.3:n.*1303C>T