Canonical Allele Identifier: CA470671690

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725217T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965460T>C , CM000672.2:g.87965460T>C	GRCh38
NC_000010.10:g.89725217T>C , CM000672.1:g.89725217T>C	GRCh37
NC_000010.9:g.89715197T>C	NCBI36
NG_007466.2:g.107022T>C , LRG_311:g.107022T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1293T>C	ENSP00000514759.2:p.Ile431=
ENST00000710265.1:c.*229T>C	ENSP00000518161.1:n.*229T>C
ENST00000688158.2:n.1935T>C
ENST00000688922.2:c.*1030T>C	ENSP00000508742.2:n.*1030T>C
ENST00000700021.1:c.1155T>C	ENSP00000514757.1:p.Ile385=
ENST00000700022.1:c.*539T>C	ENSP00000514758.1:n.*539T>C
ENST00000700023.1:n.2358T>C
ENST00000700024.1:n.2592T>C
ENST00000706954.1:c.1200T>C	ENSP00000516674.1:p.Ile400=
ENST00000706955.1:c.*1235T>C	ENSP00000516675.1:n.*1235T>C
ENST00000686459.1:c.*786T>C	ENSP00000508909.1:n.*786T>C
ENST00000688158.1:c.*1311T>C	ENSP00000509254.1:n.*1311T>C
ENST00000688308.1:c.1200T>C	ENSP00000508752.1:p.Ile400=
ENST00000688922.1:c.1121T>C
ENST00000693560.1:c.1719T>C	ENSP00000509861.1:p.Ile573=
ENST00000371953.8:c.1200T>C MANE Select	ENSP00000361021.3:p.Ile400=
ENST00000371953.7:c.1200T>C	ENSP00000361021.3:p.Ile400=
NM_000314.5:c.1200T>C	NP_000305.3:p.Ile400=
NM_000314.6:c.1200T>C	NP_000305.3:p.Ile400=
NM_001304717.2:c.1719T>C	NP_001291646.2:p.Ile573=
NM_001304718.1:c.609T>C	NP_001291647.1:p.Ile203=
XM_006717926.2:c.1155T>C	XP_006717989.1:p.Ile385=
XM_011539982.1:c.1104T>C	XP_011538284.1:p.Ile368=
XR_945791.1:n.1770T>C
NM_000314.7:c.1200T>C	NP_000305.3:p.Ile400=
NM_001304717.5:c.1719T>C	NP_001291646.4:p.Ile573=
NM_001304718.2:c.609T>C	NP_001291647.1:p.Ile203=
NM_000314.8:c.1200T>C MANE Select	NP_000305.3:p.Ile400=