Canonical Allele Identifier: CA377482823

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89693002C>A (hg19) ; chr10:g.87933245C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933245C>A , CM000672.2:g.87933245C>A	GRCh38
NC_000010.10:g.89693002C>A , CM000672.1:g.89693002C>A	GRCh37
NC_000010.9:g.89682982C>A	NCBI36
NG_007466.2:g.74807C>A , LRG_311:g.74807C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.486C>A	ENSP00000514759.2:p.Asp162Glu
ENST00000710265.1:c.486C>A	ENSP00000518161.1:p.Asp162Glu
ENST00000472832.3:c.486C>A	ENSP00000483066.2:p.Asp162Glu
ENST00000688158.2:n.1221C>A
ENST00000688922.2:c.*316C>A	ENSP00000508742.2:n.*316C>A
ENST00000700021.1:c.441C>A	ENSP00000514757.1:p.Asp147Glu
ENST00000700022.1:c.486C>A	ENSP00000514758.1:p.Asp162Glu
ENST00000700029.1:c.320C>A
ENST00000706954.1:c.486C>A	ENSP00000516674.1:p.Asp162Glu
ENST00000706955.1:c.*521C>A	ENSP00000516675.1:n.*521C>A
ENST00000686459.1:c.486C>A	ENSP00000508909.1:p.Asp162Glu
ENST00000688158.1:c.*597C>A	ENSP00000509254.1:n.*597C>A
ENST00000688308.1:c.486C>A	ENSP00000508752.1:p.Asp162Glu
ENST00000688922.1:c.407C>A
ENST00000693560.1:c.1005C>A	ENSP00000509861.1:p.Asp335Glu
ENST00000371953.8:c.486C>A MANE Select	ENSP00000361021.3:p.Asp162Glu
ENST00000371953.7:c.486C>A	ENSP00000361021.3:p.Asp162Glu
ENST00000498703.1:n.312C>A
ENST00000610634.1:c.384C>A	ENSP00000477517.1:p.Asp128Glu
NM_000314.5:c.486C>A	NP_000305.3:p.Asp162Glu
NM_000314.6:c.486C>A	NP_000305.3:p.Asp162Glu
NM_001304717.2:c.1005C>A	NP_001291646.2:p.Asp335Glu
NM_001304718.1:c.-265C>A	NP_001291647.1:n.-265C>A
XM_006717926.2:c.441C>A	XP_006717989.1:p.Asp147Glu
XM_011539981.1:c.486C>A	XP_011538283.1:p.Asp162Glu
XM_011539982.1:c.390C>A	XP_011538284.1:p.Asp130Glu
XR_945789.1:n.1198C>A
XR_945790.1:n.1198C>A
XR_945791.1:n.1198C>A
NM_000314.7:c.486C>A	NP_000305.3:p.Asp162Glu
NM_001304717.5:c.1005C>A	NP_001291646.4:p.Asp335Glu
NM_001304718.2:c.-265C>A	NP_001291647.1:n.-265C>A
NM_000314.8:c.486C>A MANE Select	NP_000305.3:p.Asp162Glu