Canonical Allele Identifier: CA470670763

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725046G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965289G>C , CM000672.2:g.87965289G>C	GRCh38
NC_000010.10:g.89725046G>C , CM000672.1:g.89725046G>C	GRCh37
NC_000010.9:g.89715026G>C	NCBI36
NG_007466.2:g.106851G>C , LRG_311:g.106851G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1122G>C	ENSP00000514759.2:p.Val374=
ENST00000710265.1:c.*58G>C	ENSP00000518161.1:n.*58G>C
ENST00000688158.2:n.1764G>C
ENST00000688922.2:c.*859G>C	ENSP00000508742.2:n.*859G>C
ENST00000700021.1:c.984G>C	ENSP00000514757.1:p.Val328=
ENST00000700022.1:c.*368G>C	ENSP00000514758.1:n.*368G>C
ENST00000700023.1:n.2187G>C
ENST00000700024.1:n.2421G>C
ENST00000706954.1:c.1029G>C	ENSP00000516674.1:p.Val343=
ENST00000706955.1:c.*1064G>C	ENSP00000516675.1:n.*1064G>C
ENST00000686459.1:c.*615G>C	ENSP00000508909.1:n.*615G>C
ENST00000688158.1:c.*1140G>C	ENSP00000509254.1:n.*1140G>C
ENST00000688308.1:c.1029G>C	ENSP00000508752.1:p.Val343=
ENST00000688922.1:c.950G>C
ENST00000693560.1:c.1548G>C	ENSP00000509861.1:p.Val516=
ENST00000371953.8:c.1029G>C MANE Select	ENSP00000361021.3:p.Val343=
ENST00000371953.7:c.1029G>C	ENSP00000361021.3:p.Val343=
NM_000314.5:c.1029G>C	NP_000305.3:p.Val343=
NM_000314.6:c.1029G>C	NP_000305.3:p.Val343=
NM_001304717.2:c.1548G>C	NP_001291646.2:p.Val516=
NM_001304718.1:c.438G>C	NP_001291647.1:p.Val146=
XM_006717926.2:c.984G>C	XP_006717989.1:p.Val328=
XM_011539982.1:c.933G>C	XP_011538284.1:p.Val311=
XR_945791.1:n.1599G>C
NM_000314.7:c.1029G>C	NP_000305.3:p.Val343=
NM_001304717.5:c.1548G>C	NP_001291646.4:p.Val516=
NM_001304718.2:c.438G>C	NP_001291647.1:p.Val146=
NM_000314.8:c.1029G>C MANE Select	NP_000305.3:p.Val343=