Canonical Allele Identifier: CA891840476

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957885_87957886delinsTG , CM000672.2:g.87957885_87957886delinsTG	GRCh38
NC_000010.10:g.89717642_89717643delinsTG , CM000672.1:g.89717642_89717643delinsTG	GRCh37
NC_000010.9:g.89707622_89707623delinsTG	NCBI36
NG_007466.2:g.99447_99448delinsTG , LRG_311:g.99447_99448delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.667_668delinsTG	ENSP00000514759.2:p.Lys223Trp
ENST00000710265.1:c.667_668delinsTG	ENSP00000518161.1:p.Lys223Trp
ENST00000472832.3:c.667_668delinsTG	ENSP00000483066.2:p.Lys223Trp
ENST00000688158.2:n.1402_1403delinsTG
ENST00000688922.2:c.*497_*498delinsTG	ENSP00000508742.2:n.*497_*498delinsTG
ENST00000700021.1:c.622_623delinsTG	ENSP00000514757.1:p.Lys208Trp
ENST00000700022.1:c.*6_*7delinsTG	ENSP00000514758.1:n.*6_*7delinsTG
ENST00000700023.1:n.1825_1826delinsTG
ENST00000700024.1:n.2059_2060delinsTG
ENST00000700025.1:n.1436_1437delinsTG
ENST00000700026.1:n.304_305delinsTG
ENST00000700029.1:c.501_502delinsTG
ENST00000706954.1:c.667_668delinsTG	ENSP00000516674.1:p.Lys223Trp
ENST00000706955.1:c.*702_*703delinsTG	ENSP00000516675.1:n.*702_*703delinsTG
ENST00000686459.1:c.*253_*254delinsTG	ENSP00000508909.1:n.*253_*254delinsTG
ENST00000688158.1:c.*778_*779delinsTG	ENSP00000509254.1:n.*778_*779delinsTG
ENST00000688308.1:c.667_668delinsTG	ENSP00000508752.1:p.Lys223Trp
ENST00000688922.1:c.588_589delinsTG
ENST00000693560.1:c.1186_1187delinsTG	ENSP00000509861.1:p.Lys396Trp
ENST00000371953.8:c.667_668delinsTG MANE Select	ENSP00000361021.3:p.Lys223Trp
ENST00000371953.7:c.667_668delinsTG	ENSP00000361021.3:p.Lys223Trp
ENST00000472832.2:c.94_95delinsTG	ENSP00000483066.1:p.Lys32Trp
NM_000314.5:c.667_668delinsTG	NP_000305.3:p.Lys223Trp
NM_000314.6:c.667_668delinsTG	NP_000305.3:p.Lys223Trp
NM_001304717.2:c.1186_1187delinsTG	NP_001291646.2:p.Lys396Trp
NM_001304718.1:c.76_77delinsTG	NP_001291647.1:p.Lys26Trp
XM_006717926.2:c.622_623delinsTG	XP_006717989.1:p.Lys208Trp
XM_011539981.1:c.667_668delinsTG	XP_011538283.1:p.Lys223Trp
XM_011539982.1:c.571_572delinsTG	XP_011538284.1:p.Lys191Trp
XR_945791.1:n.1237_1238delinsTG
NM_000314.7:c.667_668delinsTG	NP_000305.3:p.Lys223Trp
NM_001304717.5:c.1186_1187delinsTG	NP_001291646.4:p.Lys396Trp
NM_001304718.2:c.76_77delinsTG	NP_001291647.1:p.Lys26Trp
NM_000314.8:c.667_668delinsTG MANE Select	NP_000305.3:p.Lys223Trp