Canonical Allele Identifier: CA891840159

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960894_87960896delinsATG , CM000672.2:g.87960894_87960896delinsATG	GRCh38
NC_000010.10:g.89720651_89720653delinsATG , CM000672.1:g.89720651_89720653delinsATG	GRCh37
NC_000010.9:g.89710631_89710633delinsATG	NCBI36
NG_007466.2:g.102456_102458delinsATG , LRG_311:g.102456_102458delinsATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895_897delinsATG	ENSP00000514759.2:p.Asp299Met
ENST00000710265.1:c.802_804delinsATG	ENSP00000518161.1:p.Asp268Met
ENST00000472832.3:c.802_804delinsATG	ENSP00000483066.2:p.Asp268Met
ENST00000688158.2:n.1537_1539delinsATG
ENST00000688922.2:c.*632_*634delinsATG	ENSP00000508742.2:n.*632_*634delinsATG
ENST00000700021.1:c.757_759delinsATG	ENSP00000514757.1:p.Asp253Met
ENST00000700022.1:c.*141_*143delinsATG	ENSP00000514758.1:n.*141_*143delinsATG
ENST00000700023.1:n.1960_1962delinsATG
ENST00000700024.1:n.2194_2196delinsATG
ENST00000700025.1:n.1571_1573delinsATG
ENST00000700026.1:n.439_441delinsATG
ENST00000700029.1:c.729_731delinsATG
ENST00000706954.1:c.802_804delinsATG	ENSP00000516674.1:p.Asp268Met
ENST00000706955.1:c.*837_*839delinsATG	ENSP00000516675.1:n.*837_*839delinsATG
ENST00000686459.1:c.*388_*390delinsATG	ENSP00000508909.1:n.*388_*390delinsATG
ENST00000688158.1:c.*913_*915delinsATG	ENSP00000509254.1:n.*913_*915delinsATG
ENST00000688308.1:c.802_804delinsATG	ENSP00000508752.1:p.Asp268Met
ENST00000688922.1:c.723_725delinsATG
ENST00000693560.1:c.1321_1323delinsATG	ENSP00000509861.1:p.Asp441Met
ENST00000371953.8:c.802_804delinsATG MANE Select	ENSP00000361021.3:p.Asp268Met
ENST00000371953.7:c.802_804delinsATG	ENSP00000361021.3:p.Asp268Met
ENST00000472832.2:c.229_231delinsATG	ENSP00000483066.1:p.Asp77Met
NM_000314.5:c.802_804delinsATG	NP_000305.3:p.Asp268Met
NM_000314.6:c.802_804delinsATG	NP_000305.3:p.Asp268Met
NM_001304717.2:c.1321_1323delinsATG	NP_001291646.2:p.Asp441Met
NM_001304718.1:c.211_213delinsATG	NP_001291647.1:p.Asp71Met
XM_006717926.2:c.757_759delinsATG	XP_006717989.1:p.Asp253Met
XM_011539981.1:c.802_804delinsATG	XP_011538283.1:p.Asp268Met
XM_011539982.1:c.706_708delinsATG	XP_011538284.1:p.Asp236Met
XR_945791.1:n.1372_1374delinsATG
NM_000314.7:c.802_804delinsATG	NP_000305.3:p.Asp268Met
NM_001304717.5:c.1321_1323delinsATG	NP_001291646.4:p.Asp441Met
NM_001304718.2:c.211_213delinsATG	NP_001291647.1:p.Asp71Met
NM_000314.8:c.802_804delinsATG MANE Select	NP_000305.3:p.Asp268Met