Canonical Allele Identifier: CA891837355

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965341_87965342delinsCA , CM000672.2:g.87965341_87965342delinsCA	GRCh38
NC_000010.10:g.89725098_89725099delinsCA , CM000672.1:g.89725098_89725099delinsCA	GRCh37
NC_000010.9:g.89715078_89715079delinsCA	NCBI36
NG_007466.2:g.106903_106904delinsCA , LRG_311:g.106903_106904delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1174_1175delinsCA	ENSP00000514759.2:p.Ser392His
ENST00000710265.1:c.*110_*111delinsCA	ENSP00000518161.1:n.*110_*111delinsCA
ENST00000688158.2:n.1816_1817delinsCA
ENST00000688922.2:c.*911_*912delinsCA	ENSP00000508742.2:n.*911_*912delinsCA
ENST00000700021.1:c.1036_1037delinsCA	ENSP00000514757.1:p.Ser346His
ENST00000700022.1:c.*420_*421delinsCA	ENSP00000514758.1:n.*420_*421delinsCA
ENST00000700023.1:n.2239_2240delinsCA
ENST00000700024.1:n.2473_2474delinsCA
ENST00000706954.1:c.1081_1082delinsCA	ENSP00000516674.1:p.Ser361His
ENST00000706955.1:c.*1116_*1117delinsCA	ENSP00000516675.1:n.*1116_*1117delinsCA
ENST00000686459.1:c.*667_*668delinsCA	ENSP00000508909.1:n.*667_*668delinsCA
ENST00000688158.1:c.*1192_*1193delinsCA	ENSP00000509254.1:n.*1192_*1193delinsCA
ENST00000688308.1:c.1081_1082delinsCA	ENSP00000508752.1:p.Ser361His
ENST00000688922.1:c.1002_1003delinsCA
ENST00000693560.1:c.1600_1601delinsCA	ENSP00000509861.1:p.Ser534His
ENST00000371953.8:c.1081_1082delinsCA MANE Select	ENSP00000361021.3:p.Ser361His
ENST00000371953.7:c.1081_1082delinsCA	ENSP00000361021.3:p.Ser361His
NM_000314.5:c.1081_1082delinsCA	NP_000305.3:p.Ser361His
NM_000314.6:c.1081_1082delinsCA	NP_000305.3:p.Ser361His
NM_001304717.2:c.1600_1601delinsCA	NP_001291646.2:p.Ser534His
NM_001304718.1:c.490_491delinsCA	NP_001291647.1:p.Ser164His
XM_006717926.2:c.1036_1037delinsCA	XP_006717989.1:p.Ser346His
XM_011539982.1:c.985_986delinsCA	XP_011538284.1:p.Ser329His
XR_945791.1:n.1651_1652delinsCA
NM_000314.7:c.1081_1082delinsCA	NP_000305.3:p.Ser361His
NM_001304717.5:c.1600_1601delinsCA	NP_001291646.4:p.Ser534His
NM_001304718.2:c.490_491delinsCA	NP_001291647.1:p.Ser164His
NM_000314.8:c.1081_1082delinsCA MANE Select	NP_000305.3:p.Ser361His