Canonical Allele Identifier: CA470669528

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89717668C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957911C>G , CM000672.2:g.87957911C>G	GRCh38
NC_000010.10:g.89717668C>G , CM000672.1:g.89717668C>G	GRCh37
NC_000010.9:g.89707648C>G	NCBI36
NG_007466.2:g.99473C>G , LRG_311:g.99473C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.693C>G	ENSP00000514759.2:p.Pro231=
ENST00000710265.1:c.693C>G	ENSP00000518161.1:p.Pro231=
ENST00000472832.3:c.693C>G	ENSP00000483066.2:p.Pro231=
ENST00000688158.2:n.1428C>G
ENST00000688922.2:c.*523C>G	ENSP00000508742.2:n.*523C>G
ENST00000700021.1:c.648C>G	ENSP00000514757.1:p.Pro216=
ENST00000700022.1:c.*32C>G	ENSP00000514758.1:n.*32C>G
ENST00000700023.1:n.1851C>G
ENST00000700024.1:n.2085C>G
ENST00000700025.1:n.1462C>G
ENST00000700026.1:n.330C>G
ENST00000700029.1:c.527C>G
ENST00000706954.1:c.693C>G	ENSP00000516674.1:p.Pro231=
ENST00000706955.1:c.*728C>G	ENSP00000516675.1:n.*728C>G
ENST00000686459.1:c.*279C>G	ENSP00000508909.1:n.*279C>G
ENST00000688158.1:c.*804C>G	ENSP00000509254.1:n.*804C>G
ENST00000688308.1:c.693C>G	ENSP00000508752.1:p.Pro231=
ENST00000688922.1:c.614C>G
ENST00000693560.1:c.1212C>G	ENSP00000509861.1:p.Pro404=
ENST00000371953.8:c.693C>G MANE Select	ENSP00000361021.3:p.Pro231=
ENST00000371953.7:c.693C>G	ENSP00000361021.3:p.Pro231=
ENST00000472832.2:c.120C>G	ENSP00000483066.1:p.Pro40=
NM_000314.5:c.693C>G	NP_000305.3:p.Pro231=
NM_000314.6:c.693C>G	NP_000305.3:p.Pro231=
NM_001304717.2:c.1212C>G	NP_001291646.2:p.Pro404=
NM_001304718.1:c.102C>G	NP_001291647.1:p.Pro34=
XM_006717926.2:c.648C>G	XP_006717989.1:p.Pro216=
XM_011539981.1:c.693C>G	XP_011538283.1:p.Pro231=
XM_011539982.1:c.597C>G	XP_011538284.1:p.Pro199=
XR_945791.1:n.1263C>G
NM_000314.7:c.693C>G	NP_000305.3:p.Pro231=
NM_001304717.5:c.1212C>G	NP_001291646.4:p.Pro404=
NM_001304718.2:c.102C>G	NP_001291647.1:p.Pro34=
NM_000314.8:c.693C>G MANE Select	NP_000305.3:p.Pro231=