Canonical Allele Identifier: CA470667563

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89711886T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952129T>C , CM000672.2:g.87952129T>C	GRCh38
NC_000010.10:g.89711886T>C , CM000672.1:g.89711886T>C	GRCh37
NC_000010.9:g.89701866T>C	NCBI36
NG_007466.2:g.93691T>C , LRG_311:g.93691T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.504T>C	ENSP00000514759.2:p.Ile168=
ENST00000710265.1:c.504T>C	ENSP00000518161.1:p.Ile168=
ENST00000472832.3:c.504T>C	ENSP00000483066.2:p.Ile168=
ENST00000688158.2:n.1239T>C
ENST00000688922.2:c.*334T>C	ENSP00000508742.2:n.*334T>C
ENST00000700021.1:c.459T>C	ENSP00000514757.1:p.Ile153=
ENST00000700022.1:c.493-5724T>C	ENSP00000514758.1:n.493-5724T>C
ENST00000700023.1:n.1662T>C
ENST00000700024.1:n.1896T>C
ENST00000700025.1:n.1273T>C
ENST00000700029.1:c.338T>C
ENST00000706954.1:c.504T>C	ENSP00000516674.1:p.Ile168=
ENST00000706955.1:c.*539T>C	ENSP00000516675.1:n.*539T>C
ENST00000686459.1:c.*90T>C	ENSP00000508909.1:n.*90T>C
ENST00000688158.1:c.*615T>C	ENSP00000509254.1:n.*615T>C
ENST00000688308.1:c.504T>C	ENSP00000508752.1:p.Ile168=
ENST00000688922.1:c.425T>C
ENST00000693560.1:c.1023T>C	ENSP00000509861.1:p.Ile341=
ENST00000371953.8:c.504T>C MANE Select	ENSP00000361021.3:p.Ile168=
ENST00000371953.7:c.504T>C	ENSP00000361021.3:p.Ile168=
NM_000314.5:c.504T>C	NP_000305.3:p.Ile168=
NM_000314.6:c.504T>C	NP_000305.3:p.Ile168=
NM_001304717.2:c.1023T>C	NP_001291646.2:p.Ile341=
NM_001304718.1:c.-88T>C	NP_001291647.1:n.-88T>C
XM_006717926.2:c.459T>C	XP_006717989.1:p.Ile153=
XM_011539981.1:c.504T>C	XP_011538283.1:p.Ile168=
XM_011539982.1:c.408T>C	XP_011538284.1:p.Ile136=
XR_945789.1:n.1375T>C
XR_945790.1:n.1492T>C
XR_945791.1:n.1205-5724T>C
NM_000314.7:c.504T>C	NP_000305.3:p.Ile168=
NM_001304717.5:c.1023T>C	NP_001291646.4:p.Ile341=
NM_001304718.2:c.-88T>C	NP_001291647.1:n.-88T>C
NM_000314.8:c.504T>C MANE Select	NP_000305.3:p.Ile168=