Canonical Allele Identifier: CA470973931

Gene: PTEN

Linked Data

• gnomAD v3: 10-87960935-A-T
• gnomAD v4: 10-87960935-A-T
• MyVariant Identifiers: chr10:g.89720692A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960935A>T , CM000672.2:g.87960935A>T	GRCh38
NC_000010.10:g.89720692A>T , CM000672.1:g.89720692A>T	GRCh37
NC_000010.9:g.89710672A>T	NCBI36
NG_007466.2:g.102497A>T , LRG_311:g.102497A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.936A>T	ENSP00000514759.2:p.Pro312=
ENST00000710265.1:c.843A>T	ENSP00000518161.1:p.Pro281=
ENST00000472832.3:c.843A>T	ENSP00000483066.2:p.Pro281=
ENST00000688158.2:n.1578A>T
ENST00000688922.2:c.*673A>T	ENSP00000508742.2:n.*673A>T
ENST00000700021.1:c.798A>T	ENSP00000514757.1:p.Pro266=
ENST00000700022.1:c.*182A>T	ENSP00000514758.1:n.*182A>T
ENST00000700023.1:n.2001A>T
ENST00000700024.1:n.2235A>T
ENST00000700025.1:n.1612A>T
ENST00000700026.1:n.480A>T
ENST00000700029.1:c.770A>T
ENST00000706954.1:c.843A>T	ENSP00000516674.1:p.Pro281=
ENST00000706955.1:c.*878A>T	ENSP00000516675.1:n.*878A>T
ENST00000686459.1:c.*429A>T	ENSP00000508909.1:n.*429A>T
ENST00000688158.1:c.*954A>T	ENSP00000509254.1:n.*954A>T
ENST00000688308.1:c.843A>T	ENSP00000508752.1:p.Pro281=
ENST00000688922.1:c.764A>T
ENST00000693560.1:c.1362A>T	ENSP00000509861.1:p.Pro454=
ENST00000371953.8:c.843A>T MANE Select	ENSP00000361021.3:p.Pro281=
ENST00000371953.7:c.843A>T	ENSP00000361021.3:p.Pro281=
ENST00000472832.2:c.270A>T	ENSP00000483066.1:p.Pro90=
NM_000314.5:c.843A>T	NP_000305.3:p.Pro281=
NM_000314.6:c.843A>T	NP_000305.3:p.Pro281=
NM_001304717.2:c.1362A>T	NP_001291646.2:p.Pro454=
NM_001304718.1:c.252A>T	NP_001291647.1:p.Pro84=
XM_006717926.2:c.798A>T	XP_006717989.1:p.Pro266=
XM_011539981.1:c.843A>T	XP_011538283.1:p.Pro281=
XM_011539982.1:c.747A>T	XP_011538284.1:p.Pro249=
XR_945791.1:n.1413A>T
NM_000314.7:c.843A>T	NP_000305.3:p.Pro281=
NM_001304717.5:c.1362A>T	NP_001291646.4:p.Pro454=
NM_001304718.2:c.252A>T	NP_001291647.1:p.Pro84=
NM_000314.8:c.843A>T MANE Select	NP_000305.3:p.Pro281=