Canonical Allele Identifier: CA891841660

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965425_87965426delinsCC , CM000672.2:g.87965425_87965426delinsCC	GRCh38
NC_000010.10:g.89725182_89725183delinsCC , CM000672.1:g.89725182_89725183delinsCC	GRCh37
NC_000010.9:g.89715162_89715163delinsCC	NCBI36
NG_007466.2:g.106987_106988delinsCC , LRG_311:g.106987_106988delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1258_1259delinsCC	ENSP00000514759.2:p.Asn420Pro
ENST00000710265.1:c.*194_*195delinsCC	ENSP00000518161.1:n.*194_*195delinsCC
ENST00000688158.2:n.1900_1901delinsCC
ENST00000688922.2:c.*995_*996delinsCC	ENSP00000508742.2:n.*995_*996delinsCC
ENST00000700021.1:c.1120_1121delinsCC	ENSP00000514757.1:p.Asn374Pro
ENST00000700022.1:c.*504_*505delinsCC	ENSP00000514758.1:n.*504_*505delinsCC
ENST00000700023.1:n.2323_2324delinsCC
ENST00000700024.1:n.2557_2558delinsCC
ENST00000706954.1:c.1165_1166delinsCC	ENSP00000516674.1:p.Asn389Pro
ENST00000706955.1:c.*1200_*1201delinsCC	ENSP00000516675.1:n.*1200_*1201delinsCC
ENST00000686459.1:c.*751_*752delinsCC	ENSP00000508909.1:n.*751_*752delinsCC
ENST00000688158.1:c.*1276_*1277delinsCC	ENSP00000509254.1:n.*1276_*1277delinsCC
ENST00000688308.1:c.1165_1166delinsCC	ENSP00000508752.1:p.Asn389Pro
ENST00000688922.1:c.1086_1087delinsCC
ENST00000693560.1:c.1684_1685delinsCC	ENSP00000509861.1:p.Asn562Pro
ENST00000371953.8:c.1165_1166delinsCC MANE Select	ENSP00000361021.3:p.Asn389Pro
ENST00000371953.7:c.1165_1166delinsCC	ENSP00000361021.3:p.Asn389Pro
NM_000314.5:c.1165_1166delinsCC	NP_000305.3:p.Asn389Pro
NM_000314.6:c.1165_1166delinsCC	NP_000305.3:p.Asn389Pro
NM_001304717.2:c.1684_1685delinsCC	NP_001291646.2:p.Asn562Pro
NM_001304718.1:c.574_575delinsCC	NP_001291647.1:p.Asn192Pro
XM_006717926.2:c.1120_1121delinsCC	XP_006717989.1:p.Asn374Pro
XM_011539982.1:c.1069_1070delinsCC	XP_011538284.1:p.Asn357Pro
XR_945791.1:n.1735_1736delinsCC
NM_000314.7:c.1165_1166delinsCC	NP_000305.3:p.Asn389Pro
NM_001304717.5:c.1684_1685delinsCC	NP_001291646.4:p.Asn562Pro
NM_001304718.2:c.574_575delinsCC	NP_001291647.1:p.Asn192Pro
NM_000314.8:c.1165_1166delinsCC MANE Select	NP_000305.3:p.Asn389Pro