Canonical Allele Identifier: CA891836686

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961060_87961061delinsGA , CM000672.2:g.87961060_87961061delinsGA	GRCh38
NC_000010.10:g.89720817_89720818delinsGA , CM000672.1:g.89720817_89720818delinsGA	GRCh37
NC_000010.9:g.89710797_89710798delinsGA	NCBI36
NG_007466.2:g.102622_102623delinsGA , LRG_311:g.102622_102623delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1061_1062delinsGA	ENSP00000514759.2:p.Asn354Arg
ENST00000710265.1:c.968_969delinsGA	ENSP00000518161.1:p.Asn323Arg
ENST00000472832.3:c.968_969delinsGA	ENSP00000483066.2:p.Asn323Arg
ENST00000688158.2:n.1703_1704delinsGA
ENST00000688922.2:c.*798_*799delinsGA	ENSP00000508742.2:n.*798_*799delinsGA
ENST00000700021.1:c.923_924delinsGA	ENSP00000514757.1:p.Asn308Arg
ENST00000700022.1:c.*307_*308delinsGA	ENSP00000514758.1:n.*307_*308delinsGA
ENST00000700023.1:n.2126_2127delinsGA
ENST00000700024.1:n.2360_2361delinsGA
ENST00000700025.1:n.1737_1738delinsGA
ENST00000700026.1:n.605_606delinsGA
ENST00000706954.1:c.968_969delinsGA	ENSP00000516674.1:p.Asn323Arg
ENST00000706955.1:c.*1003_*1004delinsGA	ENSP00000516675.1:n.*1003_*1004delinsGA
ENST00000686459.1:c.*554_*555delinsGA	ENSP00000508909.1:n.*554_*555delinsGA
ENST00000688158.1:c.*1079_*1080delinsGA	ENSP00000509254.1:n.*1079_*1080delinsGA
ENST00000688308.1:c.968_969delinsGA	ENSP00000508752.1:p.Asn323Arg
ENST00000688922.1:c.889_890delinsGA
ENST00000693560.1:c.1487_1488delinsGA	ENSP00000509861.1:p.Asn496Arg
ENST00000371953.8:c.968_969delinsGA MANE Select	ENSP00000361021.3:p.Asn323Arg
ENST00000371953.7:c.968_969delinsGA	ENSP00000361021.3:p.Asn323Arg
ENST00000472832.2:c.395_396delinsGA	ENSP00000483066.1:p.Asn132Arg
NM_000314.5:c.968_969delinsGA	NP_000305.3:p.Asn323Arg
NM_000314.6:c.968_969delinsGA	NP_000305.3:p.Asn323Arg
NM_001304717.2:c.1487_1488delinsGA	NP_001291646.2:p.Asn496Arg
NM_001304718.1:c.377_378delinsGA	NP_001291647.1:p.Asn126Arg
XM_006717926.2:c.923_924delinsGA	XP_006717989.1:p.Asn308Arg
XM_011539981.1:c.968_969delinsGA	XP_011538283.1:p.Asn323Arg
XM_011539982.1:c.872_873delinsGA	XP_011538284.1:p.Asn291Arg
XR_945791.1:n.1538_1539delinsGA
NM_000314.7:c.968_969delinsGA	NP_000305.3:p.Asn323Arg
NM_001304717.5:c.1487_1488delinsGA	NP_001291646.4:p.Asn496Arg
NM_001304718.2:c.377_378delinsGA	NP_001291647.1:p.Asn126Arg
NM_000314.8:c.968_969delinsGA MANE Select	NP_000305.3:p.Asn323Arg