Canonical Allele Identifier: CA891836840

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961077_87961078delinsTC , CM000672.2:g.87961077_87961078delinsTC	GRCh38
NC_000010.10:g.89720834_89720835delinsTC , CM000672.1:g.89720834_89720835delinsTC	GRCh37
NC_000010.9:g.89710814_89710815delinsTC	NCBI36
NG_007466.2:g.102639_102640delinsTC , LRG_311:g.102639_102640delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1078_1079delinsTC	ENSP00000514759.2:p.Asn360Ser
ENST00000710265.1:c.985_986delinsTC	ENSP00000518161.1:p.Asn329Ser
ENST00000472832.3:c.985_986delinsTC	ENSP00000483066.2:p.Asn329Ser
ENST00000688158.2:n.1720_1721delinsTC
ENST00000688922.2:c.*815_*816delinsTC	ENSP00000508742.2:n.*815_*816delinsTC
ENST00000700021.1:c.940_941delinsTC	ENSP00000514757.1:p.Asn314Ser
ENST00000700022.1:c.*324_*325delinsTC	ENSP00000514758.1:n.*324_*325delinsTC
ENST00000700023.1:n.2143_2144delinsTC
ENST00000700024.1:n.2377_2378delinsTC
ENST00000700025.1:n.1754_1755delinsTC
ENST00000700026.1:n.622_623delinsTC
ENST00000706954.1:c.985_986delinsTC	ENSP00000516674.1:p.Asn329Ser
ENST00000706955.1:c.*1020_*1021delinsTC	ENSP00000516675.1:n.*1020_*1021delinsTC
ENST00000686459.1:c.*571_*572delinsTC	ENSP00000508909.1:n.*571_*572delinsTC
ENST00000688158.1:c.*1096_*1097delinsTC	ENSP00000509254.1:n.*1096_*1097delinsTC
ENST00000688308.1:c.985_986delinsTC	ENSP00000508752.1:p.Asn329Ser
ENST00000688922.1:c.906_907delinsTC
ENST00000693560.1:c.1504_1505delinsTC	ENSP00000509861.1:p.Asn502Ser
ENST00000371953.8:c.985_986delinsTC MANE Select	ENSP00000361021.3:p.Asn329Ser
ENST00000371953.7:c.985_986delinsTC	ENSP00000361021.3:p.Asn329Ser
ENST00000472832.2:c.412_413delinsTC	ENSP00000483066.1:p.Asn138Ser
NM_000314.5:c.985_986delinsTC	NP_000305.3:p.Asn329Ser
NM_000314.6:c.985_986delinsTC	NP_000305.3:p.Asn329Ser
NM_001304717.2:c.1504_1505delinsTC	NP_001291646.2:p.Asn502Ser
NM_001304718.1:c.394_395delinsTC	NP_001291647.1:p.Asn132Ser
XM_006717926.2:c.940_941delinsTC	XP_006717989.1:p.Asn314Ser
XM_011539981.1:c.985_986delinsTC	XP_011538283.1:p.Asn329Ser
XM_011539982.1:c.889_890delinsTC	XP_011538284.1:p.Asn297Ser
XR_945791.1:n.1555_1556delinsTC
NM_000314.7:c.985_986delinsTC	NP_000305.3:p.Asn329Ser
NM_001304717.5:c.1504_1505delinsTC	NP_001291646.4:p.Asn502Ser
NM_001304718.2:c.394_395delinsTC	NP_001291647.1:p.Asn132Ser
NM_000314.8:c.985_986delinsTC MANE Select	NP_000305.3:p.Asn329Ser