Canonical Allele Identifier: CA891840627

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957909_87957910delinsTG , CM000672.2:g.87957909_87957910delinsTG	GRCh38
NC_000010.10:g.89717666_89717667delinsTG , CM000672.1:g.89717666_89717667delinsTG	GRCh37
NC_000010.9:g.89707646_89707647delinsTG	NCBI36
NG_007466.2:g.99471_99472delinsTG , LRG_311:g.99471_99472delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.691_692delinsTG	ENSP00000514759.2:p.Pro231Cys
ENST00000710265.1:c.691_692delinsTG	ENSP00000518161.1:p.Pro231Cys
ENST00000472832.3:c.691_692delinsTG	ENSP00000483066.2:p.Pro231Cys
ENST00000688158.2:n.1426_1427delinsTG
ENST00000688922.2:c.*521_*522delinsTG	ENSP00000508742.2:n.*521_*522delinsTG
ENST00000700021.1:c.646_647delinsTG	ENSP00000514757.1:p.Pro216Cys
ENST00000700022.1:c.*30_*31delinsTG	ENSP00000514758.1:n.*30_*31delinsTG
ENST00000700023.1:n.1849_1850delinsTG
ENST00000700024.1:n.2083_2084delinsTG
ENST00000700025.1:n.1460_1461delinsTG
ENST00000700026.1:n.328_329delinsTG
ENST00000700029.1:c.525_526delinsTG
ENST00000706954.1:c.691_692delinsTG	ENSP00000516674.1:p.Pro231Cys
ENST00000706955.1:c.*726_*727delinsTG	ENSP00000516675.1:n.*726_*727delinsTG
ENST00000686459.1:c.*277_*278delinsTG	ENSP00000508909.1:n.*277_*278delinsTG
ENST00000688158.1:c.*802_*803delinsTG	ENSP00000509254.1:n.*802_*803delinsTG
ENST00000688308.1:c.691_692delinsTG	ENSP00000508752.1:p.Pro231Cys
ENST00000688922.1:c.612_613delinsTG
ENST00000693560.1:c.1210_1211delinsTG	ENSP00000509861.1:p.Pro404Cys
ENST00000371953.8:c.691_692delinsTG MANE Select	ENSP00000361021.3:p.Pro231Cys
ENST00000371953.7:c.691_692delinsTG	ENSP00000361021.3:p.Pro231Cys
ENST00000472832.2:c.118_119delinsTG	ENSP00000483066.1:p.Pro40Cys
NM_000314.5:c.691_692delinsTG	NP_000305.3:p.Pro231Cys
NM_000314.6:c.691_692delinsTG	NP_000305.3:p.Pro231Cys
NM_001304717.2:c.1210_1211delinsTG	NP_001291646.2:p.Pro404Cys
NM_001304718.1:c.100_101delinsTG	NP_001291647.1:p.Pro34Cys
XM_006717926.2:c.646_647delinsTG	XP_006717989.1:p.Pro216Cys
XM_011539981.1:c.691_692delinsTG	XP_011538283.1:p.Pro231Cys
XM_011539982.1:c.595_596delinsTG	XP_011538284.1:p.Pro199Cys
XR_945791.1:n.1261_1262delinsTG
NM_000314.7:c.691_692delinsTG	NP_000305.3:p.Pro231Cys
NM_001304717.5:c.1210_1211delinsTG	NP_001291646.4:p.Pro404Cys
NM_001304718.2:c.100_101delinsTG	NP_001291647.1:p.Pro34Cys
NM_000314.8:c.691_692delinsTG MANE Select	NP_000305.3:p.Pro231Cys