Canonical Allele Identifier: CA891841288

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952148_87952150delinsGTG , CM000672.2:g.87952148_87952150delinsGTG	GRCh38
NC_000010.10:g.89711905_89711907delinsGTG , CM000672.1:g.89711905_89711907delinsGTG	GRCh37
NC_000010.9:g.89701885_89701887delinsGTG	NCBI36
NG_007466.2:g.93710_93712delinsGTG , LRG_311:g.93710_93712delinsGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.523_525delinsGTG	ENSP00000514759.2:p.Val175=
ENST00000710265.1:c.523_525delinsGTG	ENSP00000518161.1:p.Val175=
ENST00000472832.3:c.523_525delinsGTG	ENSP00000483066.2:p.Val175=
ENST00000688158.2:n.1258_1260delinsGTG
ENST00000688922.2:c.*353_*355delinsGTG	ENSP00000508742.2:n.*353_*355delinsGTG
ENST00000700021.1:c.478_480delinsGTG	ENSP00000514757.1:p.Val160=
ENST00000700022.1:c.493-5705_493-5703delinsGTG	ENSP00000514758.1:n.493-5705_493-5703delinsGTG
ENST00000700023.1:n.1681_1683delinsGTG
ENST00000700024.1:n.1915_1917delinsGTG
ENST00000700025.1:n.1292_1294delinsGTG
ENST00000700029.1:c.357_359delinsGTG
ENST00000706954.1:c.523_525delinsGTG	ENSP00000516674.1:p.Val175=
ENST00000706955.1:c.*558_*560delinsGTG	ENSP00000516675.1:n.*558_*560delinsGTG
ENST00000686459.1:c.*109_*111delinsGTG	ENSP00000508909.1:n.*109_*111delinsGTG
ENST00000688158.1:c.*634_*636delinsGTG	ENSP00000509254.1:n.*634_*636delinsGTG
ENST00000688308.1:c.523_525delinsGTG	ENSP00000508752.1:p.Val175=
ENST00000688922.1:c.444_446delinsGTG
ENST00000693560.1:c.1042_1044delinsGTG	ENSP00000509861.1:p.Val348=
ENST00000371953.8:c.523_525delinsGTG MANE Select	ENSP00000361021.3:p.Val175=
ENST00000371953.7:c.523_525delinsGTG	ENSP00000361021.3:p.Val175=
NM_000314.5:c.523_525delinsGTG	NP_000305.3:p.Val175=
NM_000314.6:c.523_525delinsGTG	NP_000305.3:p.Val175=
NM_001304717.2:c.1042_1044delinsGTG	NP_001291646.2:p.Val348=
NM_001304718.1:c.-69_-67delinsGTG	NP_001291647.1:n.-69_-67delinsGTG
XM_006717926.2:c.478_480delinsGTG	XP_006717989.1:p.Val160=
XM_011539981.1:c.523_525delinsGTG	XP_011538283.1:p.Val175=
XM_011539982.1:c.427_429delinsGTG	XP_011538284.1:p.Val143=
XR_945789.1:n.1394_1396delinsGTG
XR_945790.1:n.1511_1513delinsGTG
XR_945791.1:n.1205-5705_1205-5703delinsGTG
NM_000314.7:c.523_525delinsGTG	NP_000305.3:p.Val175=
NM_001304717.5:c.1042_1044delinsGTG	NP_001291646.4:p.Val348=
NM_001304718.2:c.-69_-67delinsGTG	NP_001291647.1:n.-69_-67delinsGTG
NM_000314.8:c.523_525delinsGTG MANE Select	NP_000305.3:p.Val175=