Canonical Allele Identifier: CA211491246

Gene: PTEN

Linked Data

• dbSNP Id: rs186850773
• gnomAD v3: 10-87926344-C-T
• gnomAD v4: 10-87926344-C-T
• MyVariant Identifiers: chr10:g.89686101C>T (hg19) ; chr10:g.87926344C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87926344C>T , CM000672.2:g.87926344C>T	GRCh38
NC_000010.10:g.89686101C>T , CM000672.1:g.89686101C>T	GRCh37
NC_000010.9:g.89676081C>T	NCBI36
NG_007466.2:g.67906C>T , LRG_311:g.67906C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.209+787C>T	ENSP00000514759.2:n.209+787C>T
ENST00000710265.1:c.209+787C>T	ENSP00000518161.1:n.209+787C>T
ENST00000472832.3:c.209+787C>T	ENSP00000483066.2:n.209+787C>T
ENST00000688158.2:n.944+787C>T
ENST00000688922.2:c.209+787C>T	ENSP00000508742.2:n.209+787C>T
ENST00000700021.1:c.165-4702C>T	ENSP00000514757.1:n.165-4702C>T
ENST00000700022.1:c.209+787C>T	ENSP00000514758.1:n.209+787C>T
ENST00000700029.1:c.43+787C>T
ENST00000706954.1:c.209+787C>T	ENSP00000516674.1:n.209+787C>T
ENST00000706955.1:c.*244+787C>T	ENSP00000516675.1:n.*244+787C>T
ENST00000686459.1:c.209+787C>T	ENSP00000508909.1:n.209+787C>T
ENST00000688158.1:c.*320+787C>T	ENSP00000509254.1:n.*320+787C>T
ENST00000688308.1:c.209+787C>T	ENSP00000508752.1:n.209+787C>T
ENST00000688922.1:c.78+787C>T
ENST00000693560.1:c.728+787C>T	ENSP00000509861.1:n.728+787C>T
ENST00000371953.8:c.209+787C>T MANE Select	ENSP00000361021.3:n.209+787C>T
ENST00000371953.7:c.209+787C>T	ENSP00000361021.3:n.209+787C>T
ENST00000498703.1:n.35+787C>T
ENST00000610634.1:c.107+787C>T	ENSP00000477517.1:n.107+787C>T
NM_000314.5:c.209+787C>T	NP_000305.3:n.209+787C>T
NM_000314.6:c.209+787C>T	NP_000305.3:n.209+787C>T
NM_001304717.2:c.728+787C>T	NP_001291646.2:n.728+787C>T
NM_001304718.1:c.-541-4702C>T	NP_001291647.1:n.-541-4702C>T
XM_006717926.2:c.165-4702C>T	XP_006717989.1:n.165-4702C>T
XM_011539981.1:c.209+787C>T	XP_011538283.1:n.209+787C>T
XM_011539982.1:c.113+787C>T	XP_011538284.1:n.113+787C>T
XR_945789.1:n.921+787C>T
XR_945790.1:n.921+787C>T
XR_945791.1:n.921+787C>T
NM_000314.7:c.209+787C>T	NP_000305.3:n.209+787C>T
NM_001304717.5:c.728+787C>T	NP_001291646.4:n.728+787C>T
NM_001304718.2:c.-541-4702C>T	NP_001291647.1:n.-541-4702C>T
NM_000314.8:c.209+787C>T MANE Select	NP_000305.3:n.209+787C>T