Canonical Allele Identifier: CA377782023

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87864537T>C , CM000672.2:g.87864537T>C	GRCh38
NC_000010.10:g.89624294T>C , CM000672.1:g.89624294T>C	GRCh37
NC_000010.9:g.89614274T>C	NCBI36
NG_007466.2:g.6099T>C , LRG_311:g.6099T>C
NG_033079.1:g.3901A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000314.8:c.68T>C MANE Select	NP_000305.3:p.Leu23Ser
ENST00000371953.8:c.68T>C MANE Select	ENSP00000361021.3:p.Leu23Ser
NM_000314.5:c.68T>C	NP_000305.3:p.Leu23Ser
NM_000314.6:c.68T>C	NP_000305.3:p.Leu23Ser
NM_000314.7:c.68T>C	NP_000305.3:p.Leu23Ser
NM_001304717.2:c.587T>C	NP_001291646.2:p.Leu196Ser
NM_001304717.5:c.587T>C	NP_001291646.4:p.Leu196Ser
NM_001304718.1:c.-638T>C	NP_001291647.1:n.-638T>C
NM_001304718.2:c.-638T>C	NP_001291647.1:n.-638T>C
ENST00000371953.7:c.68T>C	ENSP00000361021.3:p.Leu23Ser
ENST00000462694.1:n.70T>C
ENST00000472832.3:c.68T>C	ENSP00000483066.2:p.Leu23Ser
ENST00000487939.1:n.89T>C
ENST00000610634.1:c.-35T>C	ENSP00000477517.1:n.-35T>C
ENST00000618586.1:n.37T>C
ENST00000686459.1:c.68T>C	ENSP00000508909.1:p.Leu23Ser
ENST00000688158.1:c.68T>C	ENSP00000509254.1:p.Leu23Ser
ENST00000688308.1:c.68T>C	ENSP00000508752.1:p.Leu23Ser
ENST00000688922.2:c.68T>C	ENSP00000508742.2:p.Leu23Ser
ENST00000693560.1:c.587T>C	ENSP00000509861.1:p.Leu196Ser
ENST00000700021.1:c.68T>C	ENSP00000514757.1:p.Leu23Ser
ENST00000700022.1:c.68T>C	ENSP00000514758.1:p.Leu23Ser
ENST00000700029.2:c.68T>C	ENSP00000514759.2:p.Leu23Ser
ENST00000706954.1:c.68T>C	ENSP00000516674.1:p.Leu23Ser
ENST00000706955.1:c.68T>C	ENSP00000516675.1:p.Leu23Ser
ENST00000710265.1:c.68T>C	ENSP00000518161.1:p.Leu23Ser
XM_006717926.2:c.68T>C	XP_006717989.1:p.Leu23Ser
XM_011539981.1:c.68T>C	XP_011538283.1:p.Leu23Ser
XR_945789.1:n.780T>C
XR_945790.1:n.780T>C
XR_945791.1:n.780T>C