Canonical Allele Identifier: CA891837050

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965311_87965312delinsCA , CM000672.2:g.87965311_87965312delinsCA	GRCh38
NC_000010.10:g.89725068_89725069delinsCA , CM000672.1:g.89725068_89725069delinsCA	GRCh37
NC_000010.9:g.89715048_89715049delinsCA	NCBI36
NG_007466.2:g.106873_106874delinsCA , LRG_311:g.106873_106874delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1144_1145delinsCA	ENSP00000514759.2:p.Val382Gln
ENST00000710265.1:c.*80_*81delinsCA	ENSP00000518161.1:n.*80_*81delinsCA
ENST00000688158.2:n.1786_1787delinsCA
ENST00000688922.2:c.*881_*882delinsCA	ENSP00000508742.2:n.*881_*882delinsCA
ENST00000700021.1:c.1006_1007delinsCA	ENSP00000514757.1:p.Val336Gln
ENST00000700022.1:c.*390_*391delinsCA	ENSP00000514758.1:n.*390_*391delinsCA
ENST00000700023.1:n.2209_2210delinsCA
ENST00000700024.1:n.2443_2444delinsCA
ENST00000706954.1:c.1051_1052delinsCA	ENSP00000516674.1:p.Val351Gln
ENST00000706955.1:c.*1086_*1087delinsCA	ENSP00000516675.1:n.*1086_*1087delinsCA
ENST00000686459.1:c.*637_*638delinsCA	ENSP00000508909.1:n.*637_*638delinsCA
ENST00000688158.1:c.*1162_*1163delinsCA	ENSP00000509254.1:n.*1162_*1163delinsCA
ENST00000688308.1:c.1051_1052delinsCA	ENSP00000508752.1:p.Val351Gln
ENST00000688922.1:c.972_973delinsCA
ENST00000693560.1:c.1570_1571delinsCA	ENSP00000509861.1:p.Val524Gln
ENST00000371953.8:c.1051_1052delinsCA MANE Select	ENSP00000361021.3:p.Val351Gln
ENST00000371953.7:c.1051_1052delinsCA	ENSP00000361021.3:p.Val351Gln
NM_000314.5:c.1051_1052delinsCA	NP_000305.3:p.Val351Gln
NM_000314.6:c.1051_1052delinsCA	NP_000305.3:p.Val351Gln
NM_001304717.2:c.1570_1571delinsCA	NP_001291646.2:p.Val524Gln
NM_001304718.1:c.460_461delinsCA	NP_001291647.1:p.Val154Gln
XM_006717926.2:c.1006_1007delinsCA	XP_006717989.1:p.Val336Gln
XM_011539982.1:c.955_956delinsCA	XP_011538284.1:p.Val319Gln
XR_945791.1:n.1621_1622delinsCA
NM_000314.7:c.1051_1052delinsCA	NP_000305.3:p.Val351Gln
NM_001304717.5:c.1570_1571delinsCA	NP_001291646.4:p.Val524Gln
NM_001304718.2:c.460_461delinsCA	NP_001291647.1:p.Val154Gln
NM_000314.8:c.1051_1052delinsCA MANE Select	NP_000305.3:p.Val351Gln