Canonical Allele Identifier: CA470671386

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725149A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965392A>C , CM000672.2:g.87965392A>C	GRCh38
NC_000010.10:g.89725149A>C , CM000672.1:g.89725149A>C	GRCh37
NC_000010.9:g.89715129A>C	NCBI36
NG_007466.2:g.106954A>C , LRG_311:g.106954A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1225A>C	ENSP00000514759.2:p.Arg409=
ENST00000710265.1:c.*161A>C	ENSP00000518161.1:n.*161A>C
ENST00000688158.2:n.1867A>C
ENST00000688922.2:c.*962A>C	ENSP00000508742.2:n.*962A>C
ENST00000700021.1:c.1087A>C	ENSP00000514757.1:p.Arg363=
ENST00000700022.1:c.*471A>C	ENSP00000514758.1:n.*471A>C
ENST00000700023.1:n.2290A>C
ENST00000700024.1:n.2524A>C
ENST00000706954.1:c.1132A>C	ENSP00000516674.1:p.Arg378=
ENST00000706955.1:c.*1167A>C	ENSP00000516675.1:n.*1167A>C
ENST00000686459.1:c.*718A>C	ENSP00000508909.1:n.*718A>C
ENST00000688158.1:c.*1243A>C	ENSP00000509254.1:n.*1243A>C
ENST00000688308.1:c.1132A>C	ENSP00000508752.1:p.Arg378=
ENST00000688922.1:c.1053A>C
ENST00000693560.1:c.1651A>C	ENSP00000509861.1:p.Arg551=
ENST00000371953.8:c.1132A>C MANE Select	ENSP00000361021.3:p.Arg378=
ENST00000371953.7:c.1132A>C	ENSP00000361021.3:p.Arg378=
NM_000314.5:c.1132A>C	NP_000305.3:p.Arg378=
NM_000314.6:c.1132A>C	NP_000305.3:p.Arg378=
NM_001304717.2:c.1651A>C	NP_001291646.2:p.Arg551=
NM_001304718.1:c.541A>C	NP_001291647.1:p.Arg181=
XM_006717926.2:c.1087A>C	XP_006717989.1:p.Arg363=
XM_011539982.1:c.1036A>C	XP_011538284.1:p.Arg346=
XR_945791.1:n.1702A>C
NM_000314.7:c.1132A>C	NP_000305.3:p.Arg378=
NM_001304717.5:c.1651A>C	NP_001291646.4:p.Arg551=
NM_001304718.2:c.541A>C	NP_001291647.1:p.Arg181=
NM_000314.8:c.1132A>C MANE Select	NP_000305.3:p.Arg378=