Canonical Allele Identifier: CA891838720

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952140_87952141delinsCT , CM000672.2:g.87952140_87952141delinsCT	GRCh38
NC_000010.10:g.89711897_89711898delinsCT , CM000672.1:g.89711897_89711898delinsCT	GRCh37
NC_000010.9:g.89701877_89701878delinsCT	NCBI36
NG_007466.2:g.93702_93703delinsCT , LRG_311:g.93702_93703delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.515_516delinsCT	ENSP00000514759.2:p.Arg172Thr
ENST00000710265.1:c.515_516delinsCT	ENSP00000518161.1:p.Arg172Thr
ENST00000472832.3:c.515_516delinsCT	ENSP00000483066.2:p.Arg172Thr
ENST00000688158.2:n.1250_1251delinsCT
ENST00000688922.2:c.*345_*346delinsCT	ENSP00000508742.2:n.*345_*346delinsCT
ENST00000700021.1:c.470_471delinsCT	ENSP00000514757.1:p.Arg157Thr
ENST00000700022.1:c.493-5713_493-5712delinsCT	ENSP00000514758.1:n.493-5713_493-5712delinsCT
ENST00000700023.1:n.1673_1674delinsCT
ENST00000700024.1:n.1907_1908delinsCT
ENST00000700025.1:n.1284_1285delinsCT
ENST00000700029.1:c.349_350delinsCT
ENST00000706954.1:c.515_516delinsCT	ENSP00000516674.1:p.Arg172Thr
ENST00000706955.1:c.*550_*551delinsCT	ENSP00000516675.1:n.*550_*551delinsCT
ENST00000686459.1:c.*101_*102delinsCT	ENSP00000508909.1:n.*101_*102delinsCT
ENST00000688158.1:c.*626_*627delinsCT	ENSP00000509254.1:n.*626_*627delinsCT
ENST00000688308.1:c.515_516delinsCT	ENSP00000508752.1:p.Arg172Thr
ENST00000688922.1:c.436_437delinsCT
ENST00000693560.1:c.1034_1035delinsCT	ENSP00000509861.1:p.Arg345Thr
ENST00000371953.8:c.515_516delinsCT MANE Select	ENSP00000361021.3:p.Arg172Thr
ENST00000371953.7:c.515_516delinsCT	ENSP00000361021.3:p.Arg172Thr
NM_000314.5:c.515_516delinsCT	NP_000305.3:p.Arg172Thr
NM_000314.6:c.515_516delinsCT	NP_000305.3:p.Arg172Thr
NM_001304717.2:c.1034_1035delinsCT	NP_001291646.2:p.Arg345Thr
NM_001304718.1:c.-77_-76delinsCT	NP_001291647.1:n.-77_-76delinsCT
XM_006717926.2:c.470_471delinsCT	XP_006717989.1:p.Arg157Thr
XM_011539981.1:c.515_516delinsCT	XP_011538283.1:p.Arg172Thr
XM_011539982.1:c.419_420delinsCT	XP_011538284.1:p.Arg140Thr
XR_945789.1:n.1386_1387delinsCT
XR_945790.1:n.1503_1504delinsCT
XR_945791.1:n.1205-5713_1205-5712delinsCT
NM_000314.7:c.515_516delinsCT	NP_000305.3:p.Arg172Thr
NM_001304717.5:c.1034_1035delinsCT	NP_001291646.4:p.Arg345Thr
NM_001304718.2:c.-77_-76delinsCT	NP_001291647.1:n.-77_-76delinsCT
NM_000314.8:c.515_516delinsCT MANE Select	NP_000305.3:p.Arg172Thr