Canonical Allele Identifier: CA470973973

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960979_87960980insA , CM000672.2:g.87960979_87960980insA	GRCh38
NC_000010.10:g.89720736_89720737insA , CM000672.1:g.89720736_89720737insA	GRCh37
NC_000010.9:g.89710716_89710717insA	NCBI36
NG_007466.2:g.102541_102542insA , LRG_311:g.102541_102542insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.980_981insA	ENSP00000514759.2:p.Cys327Ter
ENST00000710265.1:c.887_888insA	ENSP00000518161.1:p.Cys296Ter
ENST00000472832.3:c.887_888insA	ENSP00000483066.2:p.Cys296Ter
ENST00000688158.2:n.1622_1623insA
ENST00000688922.2:c.*717_*718insA	ENSP00000508742.2:n.*717_*718insA
ENST00000700021.1:c.842_843insA	ENSP00000514757.1:p.Cys281Ter
ENST00000700022.1:c.*226_*227insA	ENSP00000514758.1:n.*226_*227insA
ENST00000700023.1:n.2045_2046insA
ENST00000700024.1:n.2279_2280insA
ENST00000700025.1:n.1656_1657insA
ENST00000700026.1:n.524_525insA
ENST00000706954.1:c.887_888insA	ENSP00000516674.1:p.Cys296Ter
ENST00000706955.1:c.*922_*923insA	ENSP00000516675.1:n.*922_*923insA
ENST00000686459.1:c.*473_*474insA	ENSP00000508909.1:n.*473_*474insA
ENST00000688158.1:c.*998_*999insA	ENSP00000509254.1:n.*998_*999insA
ENST00000688308.1:c.887_888insA	ENSP00000508752.1:p.Cys296Ter
ENST00000688922.1:c.808_809insA
ENST00000693560.1:c.1406_1407insA	ENSP00000509861.1:p.Cys469Ter
ENST00000371953.8:c.887_888insA MANE Select	ENSP00000361021.3:p.Cys296Ter
ENST00000371953.7:c.887_888insA	ENSP00000361021.3:p.Cys296Ter
ENST00000472832.2:c.314_315insA	ENSP00000483066.1:p.Cys105Ter
NM_000314.5:c.887_888insA	NP_000305.3:p.Cys296Ter
NM_000314.6:c.887_888insA	NP_000305.3:p.Cys296Ter
NM_001304717.2:c.1406_1407insA	NP_001291646.2:p.Cys469Ter
NM_001304718.1:c.296_297insA	NP_001291647.1:p.Cys99Ter
XM_006717926.2:c.842_843insA	XP_006717989.1:p.Cys281Ter
XM_011539981.1:c.887_888insA	XP_011538283.1:p.Cys296Ter
XM_011539982.1:c.791_792insA	XP_011538284.1:p.Cys264Ter
XR_945791.1:n.1457_1458insA
NM_000314.7:c.887_888insA	NP_000305.3:p.Cys296Ter
NM_001304717.5:c.1406_1407insA	NP_001291646.4:p.Cys469Ter
NM_001304718.2:c.296_297insA	NP_001291647.1:p.Cys99Ter
NM_000314.8:c.887_888insA MANE Select	NP_000305.3:p.Cys296Ter