Canonical Allele Identifier: CA1926190035

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961005_87961006delinsAG , CM000672.2:g.87961005_87961006delinsAG	GRCh38
NC_000010.10:g.89720762_89720763delinsAG , CM000672.1:g.89720762_89720763delinsAG	GRCh37
NC_000010.9:g.89710742_89710743delinsAG	NCBI36
NG_007466.2:g.102567_102568delinsAG , LRG_311:g.102567_102568delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1006_1007delinsAG	ENSP00000514759.2:p.Ser336=
ENST00000710265.1:c.913_914delinsAG	ENSP00000518161.1:p.Ser305=
ENST00000472832.3:c.913_914delinsAG	ENSP00000483066.2:p.Ser305=
ENST00000688158.2:n.1648_1649delinsAG
ENST00000688922.2:c.*743_*744delinsAG	ENSP00000508742.2:n.*743_*744delinsAG
ENST00000700021.1:c.868_869delinsAG	ENSP00000514757.1:p.Ser290=
ENST00000700022.1:c.*252_*253delinsAG	ENSP00000514758.1:n.*252_*253delinsAG
ENST00000700023.1:n.2071_2072delinsAG
ENST00000700024.1:n.2305_2306delinsAG
ENST00000700025.1:n.1682_1683delinsAG
ENST00000700026.1:n.550_551delinsAG
ENST00000706954.1:c.913_914delinsAG	ENSP00000516674.1:p.Ser305=
ENST00000706955.1:c.*948_*949delinsAG	ENSP00000516675.1:n.*948_*949delinsAG
ENST00000686459.1:c.*499_*500delinsAG	ENSP00000508909.1:n.*499_*500delinsAG
ENST00000688158.1:c.*1024_*1025delinsAG	ENSP00000509254.1:n.*1024_*1025delinsAG
ENST00000688308.1:c.913_914delinsAG	ENSP00000508752.1:p.Ser305=
ENST00000688922.1:c.834_835delinsAG
ENST00000693560.1:c.1432_1433delinsAG	ENSP00000509861.1:p.Ser478=
ENST00000371953.8:c.913_914delinsAG MANE Select	ENSP00000361021.3:p.Ser305=
ENST00000371953.7:c.913_914delinsAG	ENSP00000361021.3:p.Ser305=
ENST00000472832.2:c.340_341delinsAG	ENSP00000483066.1:p.Ser114=
NM_000314.5:c.913_914delinsAG	NP_000305.3:p.Ser305=
NM_000314.6:c.913_914delinsAG	NP_000305.3:p.Ser305=
NM_001304717.2:c.1432_1433delinsAG	NP_001291646.2:p.Ser478=
NM_001304718.1:c.322_323delinsAG	NP_001291647.1:p.Ser108=
XM_006717926.2:c.868_869delinsAG	XP_006717989.1:p.Ser290=
XM_011539981.1:c.913_914delinsAG	XP_011538283.1:p.Ser305=
XM_011539982.1:c.817_818delinsAG	XP_011538284.1:p.Ser273=
XR_945791.1:n.1483_1484delinsAG
NM_000314.7:c.913_914delinsAG	NP_000305.3:p.Ser305=
NM_001304717.5:c.1432_1433delinsAG	NP_001291646.4:p.Ser478=
NM_001304718.2:c.322_323delinsAG	NP_001291647.1:p.Ser108=
NM_000314.8:c.913_914delinsAG MANE Select	NP_000305.3:p.Ser305=