Canonical Allele Identifier: CA470669822
Gene: PTEN HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.89717713G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957956G>C , CM000672.2:g.87957956G>C GRCh38
NC_000010.10:g.89717713G>C , CM000672.1:g.89717713G>C GRCh37
NC_000010.9:g.89707693G>C NCBI36
NG_007466.2:g.99518G>C , LRG_311:g.99518G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.738G>C ENSP00000514759.2:p.Pro246=
ENST00000710265.1:c.738G>C ENSP00000518161.1:p.Pro246=
ENST00000472832.3:c.738G>C ENSP00000483066.2:p.Pro246=
ENST00000688158.2:n.1473G>C
ENST00000688922.2:c.*568G>C ENSP00000508742.2:n.*568G>C
ENST00000700021.1:c.693G>C ENSP00000514757.1:p.Pro231=
ENST00000700022.1:c.*77G>C ENSP00000514758.1:n.*77G>C
ENST00000700023.1:n.1896G>C
ENST00000700024.1:n.2130G>C
ENST00000700025.1:n.1507G>C
ENST00000700026.1:n.375G>C
ENST00000700029.1:c.572G>C
ENST00000706954.1:c.738G>C ENSP00000516674.1:p.Pro246=
ENST00000706955.1:c.*773G>C ENSP00000516675.1:n.*773G>C
ENST00000686459.1:c.*324G>C ENSP00000508909.1:n.*324G>C
ENST00000688158.1:c.*849G>C ENSP00000509254.1:n.*849G>C
ENST00000688308.1:c.738G>C ENSP00000508752.1:p.Pro246=
ENST00000688922.1:c.659G>C
ENST00000693560.1:c.1257G>C ENSP00000509861.1:p.Pro419=
ENST00000371953.8:c.738G>C MANE Select ENSP00000361021.3:p.Pro246=
ENST00000371953.7:c.738G>C ENSP00000361021.3:p.Pro246=
ENST00000472832.2:c.165G>C ENSP00000483066.1:p.Pro55=
NM_000314.5:c.738G>C NP_000305.3:p.Pro246=
NM_000314.6:c.738G>C NP_000305.3:p.Pro246=
NM_001304717.2:c.1257G>C NP_001291646.2:p.Pro419=
NM_001304718.1:c.147G>C NP_001291647.1:p.Pro49=
XM_006717926.2:c.693G>C XP_006717989.1:p.Pro231=
XM_011539981.1:c.738G>C XP_011538283.1:p.Pro246=
XM_011539982.1:c.642G>C XP_011538284.1:p.Pro214=
XR_945791.1:n.1308G>C
NM_000314.7:c.738G>C NP_000305.3:p.Pro246=
NM_001304717.5:c.1257G>C NP_001291646.4:p.Pro419=
NM_001304718.2:c.147G>C NP_001291647.1:p.Pro49=
NM_000314.8:c.738G>C MANE Select NP_000305.3:p.Pro246=
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