Canonical Allele Identifier: CA891840230

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960909_87960911delinsATG , CM000672.2:g.87960909_87960911delinsATG	GRCh38
NC_000010.10:g.89720666_89720668delinsATG , CM000672.1:g.89720666_89720668delinsATG	GRCh37
NC_000010.9:g.89710646_89710648delinsATG	NCBI36
NG_007466.2:g.102471_102473delinsATG , LRG_311:g.102471_102473delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.910_912delinsATG	ENSP00000514759.2:p.Phe304Met
ENST00000710265.1:c.817_819delinsATG	ENSP00000518161.1:p.Phe273Met
ENST00000472832.3:c.817_819delinsATG	ENSP00000483066.2:p.Phe273Met
ENST00000688158.2:n.1552_1554delinsATG
ENST00000688922.2:c.*647_*649delinsATG	ENSP00000508742.2:n.*647_*649delinsATG
ENST00000700021.1:c.772_774delinsATG	ENSP00000514757.1:p.Phe258Met
ENST00000700022.1:c.*156_*158delinsATG	ENSP00000514758.1:n.*156_*158delinsATG
ENST00000700023.1:n.1975_1977delinsATG
ENST00000700024.1:n.2209_2211delinsATG
ENST00000700025.1:n.1586_1588delinsATG
ENST00000700026.1:n.454_456delinsATG
ENST00000700029.1:c.744_746delinsATG
ENST00000706954.1:c.817_819delinsATG	ENSP00000516674.1:p.Phe273Met
ENST00000706955.1:c.*852_*854delinsATG	ENSP00000516675.1:n.*852_*854delinsATG
ENST00000686459.1:c.*403_*405delinsATG	ENSP00000508909.1:n.*403_*405delinsATG
ENST00000688158.1:c.*928_*930delinsATG	ENSP00000509254.1:n.*928_*930delinsATG
ENST00000688308.1:c.817_819delinsATG	ENSP00000508752.1:p.Phe273Met
ENST00000688922.1:c.738_740delinsATG
ENST00000693560.1:c.1336_1338delinsATG	ENSP00000509861.1:p.Phe446Met
ENST00000371953.8:c.817_819delinsATG MANE Select	ENSP00000361021.3:p.Phe273Met
ENST00000371953.7:c.817_819delinsATG	ENSP00000361021.3:p.Phe273Met
ENST00000472832.2:c.244_246delinsATG	ENSP00000483066.1:p.Phe82Met
NM_000314.5:c.817_819delinsATG	NP_000305.3:p.Phe273Met
NM_000314.6:c.817_819delinsATG	NP_000305.3:p.Phe273Met
NM_001304717.2:c.1336_1338delinsATG	NP_001291646.2:p.Phe446Met
NM_001304718.1:c.226_228delinsATG	NP_001291647.1:p.Phe76Met
XM_006717926.2:c.772_774delinsATG	XP_006717989.1:p.Phe258Met
XM_011539981.1:c.817_819delinsATG	XP_011538283.1:p.Phe273Met
XM_011539982.1:c.721_723delinsATG	XP_011538284.1:p.Phe241Met
XR_945791.1:n.1387_1389delinsATG
NM_000314.7:c.817_819delinsATG	NP_000305.3:p.Phe273Met
NM_001304717.5:c.1336_1338delinsATG	NP_001291646.4:p.Phe446Met
NM_001304718.2:c.226_228delinsATG	NP_001291647.1:p.Phe76Met
NM_000314.8:c.817_819delinsATG MANE Select	NP_000305.3:p.Phe273Met