Canonical Allele Identifier: CA2579926477

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965305_87965307delinsTCT , CM000672.2:g.87965305_87965307delinsTCT	GRCh38
NC_000010.10:g.89725062_89725064delinsTCT , CM000672.1:g.89725062_89725064delinsTCT	GRCh37
NC_000010.9:g.89715042_89715044delinsTCT	NCBI36
NG_007466.2:g.106867_106869delinsTCT , LRG_311:g.106867_106869delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1138_1140delinsTCT	ENSP00000514759.2:p.Lys380Ser
ENST00000710265.1:c.*74_*76delinsTCT	ENSP00000518161.1:n.*74_*76delinsTCT
ENST00000688158.2:n.1780_1782delinsTCT
ENST00000688922.2:c.*875_*877delinsTCT	ENSP00000508742.2:n.*875_*877delinsTCT
ENST00000700021.1:c.1000_1002delinsTCT	ENSP00000514757.1:p.Lys334Ser
ENST00000700022.1:c.*384_*386delinsTCT	ENSP00000514758.1:n.*384_*386delinsTCT
ENST00000700023.1:n.2203_2205delinsTCT
ENST00000700024.1:n.2437_2439delinsTCT
ENST00000706954.1:c.1045_1047delinsTCT	ENSP00000516674.1:p.Lys349Ser
ENST00000706955.1:c.*1080_*1082delinsTCT	ENSP00000516675.1:n.*1080_*1082delinsTCT
ENST00000686459.1:c.*631_*633delinsTCT	ENSP00000508909.1:n.*631_*633delinsTCT
ENST00000688158.1:c.*1156_*1158delinsTCT	ENSP00000509254.1:n.*1156_*1158delinsTCT
ENST00000688308.1:c.1045_1047delinsTCT	ENSP00000508752.1:p.Lys349Ser
ENST00000688922.1:c.966_968delinsTCT
ENST00000693560.1:c.1564_1566delinsTCT	ENSP00000509861.1:p.Lys522Ser
ENST00000371953.8:c.1045_1047delinsTCT MANE Select	ENSP00000361021.3:p.Lys349Ser
ENST00000371953.7:c.1045_1047delinsTCT	ENSP00000361021.3:p.Lys349Ser
NM_000314.5:c.1045_1047delinsTCT	NP_000305.3:p.Lys349Ser
NM_000314.6:c.1045_1047delinsTCT	NP_000305.3:p.Lys349Ser
NM_001304717.2:c.1564_1566delinsTCT	NP_001291646.2:p.Lys522Ser
NM_001304718.1:c.454_456delinsTCT	NP_001291647.1:p.Lys152Ser
XM_006717926.2:c.1000_1002delinsTCT	XP_006717989.1:p.Lys334Ser
XM_011539982.1:c.949_951delinsTCT	XP_011538284.1:p.Lys317Ser
XR_945791.1:n.1615_1617delinsTCT
NM_000314.7:c.1045_1047delinsTCT	NP_000305.3:p.Lys349Ser
NM_001304717.5:c.1564_1566delinsTCT	NP_001291646.4:p.Lys522Ser
NM_001304718.2:c.454_456delinsTCT	NP_001291647.1:p.Lys152Ser
NM_000314.8:c.1045_1047delinsTCT MANE Select	NP_000305.3:p.Lys349Ser