Canonical Allele Identifier: CA377482833

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933249A>T , CM000672.2:g.87933249A>T	GRCh38
NC_000010.10:g.89693006A>T , CM000672.1:g.89693006A>T	GRCh37
NC_000010.9:g.89682986A>T	NCBI36
NG_007466.2:g.74811A>T , LRG_311:g.74811A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000314.8:c.490A>T MANE Select	NP_000305.3:p.Lys164Ter
ENST00000371953.8:c.490A>T MANE Select	ENSP00000361021.3:p.Lys164Ter
NM_000314.5:c.490A>T	NP_000305.3:p.Lys164Ter
NM_000314.6:c.490A>T	NP_000305.3:p.Lys164Ter
NM_000314.7:c.490A>T	NP_000305.3:p.Lys164Ter
NM_001304717.2:c.1009A>T	NP_001291646.2:p.Lys337Ter
NM_001304717.5:c.1009A>T	NP_001291646.4:p.Lys337Ter
NM_001304718.1:c.-261A>T	NP_001291647.1:n.-261A>T
NM_001304718.2:c.-261A>T	NP_001291647.1:n.-261A>T
ENST00000371953.7:c.490A>T	ENSP00000361021.3:p.Lys164Ter
ENST00000472832.3:c.490A>T	ENSP00000483066.2:p.Lys164Ter
ENST00000498703.1:n.316A>T
ENST00000610634.1:c.388A>T	ENSP00000477517.1:p.Lys130Ter
ENST00000686459.1:c.490A>T	ENSP00000508909.1:p.Lys164Ter
ENST00000688158.1:c.*601A>T	ENSP00000509254.1:n.*601A>T
ENST00000688158.2:n.1225A>T
ENST00000688308.1:c.490A>T	ENSP00000508752.1:p.Lys164Ter
ENST00000688922.1:c.411A>T
ENST00000688922.2:c.*320A>T	ENSP00000508742.2:n.*320A>T
ENST00000693560.1:c.1009A>T	ENSP00000509861.1:p.Lys337Ter
ENST00000700021.1:c.445A>T	ENSP00000514757.1:p.Lys149Ter
ENST00000700022.1:c.490A>T	ENSP00000514758.1:p.Lys164Ter
ENST00000700029.1:c.324A>T
ENST00000700029.2:c.490A>T	ENSP00000514759.2:p.Lys164Ter
ENST00000706954.1:c.490A>T	ENSP00000516674.1:p.Lys164Ter
ENST00000706955.1:c.*525A>T	ENSP00000516675.1:n.*525A>T
ENST00000710265.1:c.490A>T	ENSP00000518161.1:p.Lys164Ter
XM_006717926.2:c.445A>T	XP_006717989.1:p.Lys149Ter
XM_011539981.1:c.490A>T	XP_011538283.1:p.Lys164Ter
XM_011539982.1:c.394A>T	XP_011538284.1:p.Lys132Ter
XR_945789.1:n.1202A>T
XR_945790.1:n.1202A>T
XR_945791.1:n.1202A>T