Canonical Allele Identifier: CA470973985

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89720758T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961001T>C , CM000672.2:g.87961001T>C	GRCh38
NC_000010.10:g.89720758T>C , CM000672.1:g.89720758T>C	GRCh37
NC_000010.9:g.89710738T>C	NCBI36
NG_007466.2:g.102563T>C , LRG_311:g.102563T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1002T>C	ENSP00000514759.2:p.Ile334=
ENST00000710265.1:c.909T>C	ENSP00000518161.1:p.Ile303=
ENST00000472832.3:c.909T>C	ENSP00000483066.2:p.Ile303=
ENST00000688158.2:n.1644T>C
ENST00000688922.2:c.*739T>C	ENSP00000508742.2:n.*739T>C
ENST00000700021.1:c.864T>C	ENSP00000514757.1:p.Ile288=
ENST00000700022.1:c.*248T>C	ENSP00000514758.1:n.*248T>C
ENST00000700023.1:n.2067T>C
ENST00000700024.1:n.2301T>C
ENST00000700025.1:n.1678T>C
ENST00000700026.1:n.546T>C
ENST00000706954.1:c.909T>C	ENSP00000516674.1:p.Ile303=
ENST00000706955.1:c.*944T>C	ENSP00000516675.1:n.*944T>C
ENST00000686459.1:c.*495T>C	ENSP00000508909.1:n.*495T>C
ENST00000688158.1:c.*1020T>C	ENSP00000509254.1:n.*1020T>C
ENST00000688308.1:c.909T>C	ENSP00000508752.1:p.Ile303=
ENST00000688922.1:c.830T>C
ENST00000693560.1:c.1428T>C	ENSP00000509861.1:p.Ile476=
ENST00000371953.8:c.909T>C MANE Select	ENSP00000361021.3:p.Ile303=
ENST00000371953.7:c.909T>C	ENSP00000361021.3:p.Ile303=
ENST00000472832.2:c.336T>C	ENSP00000483066.1:p.Ile112=
NM_000314.5:c.909T>C	NP_000305.3:p.Ile303=
NM_000314.6:c.909T>C	NP_000305.3:p.Ile303=
NM_001304717.2:c.1428T>C	NP_001291646.2:p.Ile476=
NM_001304718.1:c.318T>C	NP_001291647.1:p.Ile106=
XM_006717926.2:c.864T>C	XP_006717989.1:p.Ile288=
XM_011539981.1:c.909T>C	XP_011538283.1:p.Ile303=
XM_011539982.1:c.813T>C	XP_011538284.1:p.Ile271=
XR_945791.1:n.1479T>C
NM_000314.7:c.909T>C	NP_000305.3:p.Ile303=
NM_001304717.5:c.1428T>C	NP_001291646.4:p.Ile476=
NM_001304718.2:c.318T>C	NP_001291647.1:p.Ile106=
NM_000314.8:c.909T>C MANE Select	NP_000305.3:p.Ile303=