Canonical Allele Identifier: CA891836738

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961065_87961066delinsTA , CM000672.2:g.87961065_87961066delinsTA	GRCh38
NC_000010.10:g.89720822_89720823delinsTA , CM000672.1:g.89720822_89720823delinsTA	GRCh37
NC_000010.9:g.89710802_89710803delinsTA	NCBI36
NG_007466.2:g.102627_102628delinsTA , LRG_311:g.102627_102628delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1066_1067delinsTA	ENSP00000514759.2:p.Leu356Tyr
ENST00000710265.1:c.973_974delinsTA	ENSP00000518161.1:p.Leu325Tyr
ENST00000472832.3:c.973_974delinsTA	ENSP00000483066.2:p.Leu325Tyr
ENST00000688158.2:n.1708_1709delinsTA
ENST00000688922.2:c.*803_*804delinsTA	ENSP00000508742.2:n.*803_*804delinsTA
ENST00000700021.1:c.928_929delinsTA	ENSP00000514757.1:p.Leu310Tyr
ENST00000700022.1:c.*312_*313delinsTA	ENSP00000514758.1:n.*312_*313delinsTA
ENST00000700023.1:n.2131_2132delinsTA
ENST00000700024.1:n.2365_2366delinsTA
ENST00000700025.1:n.1742_1743delinsTA
ENST00000700026.1:n.610_611delinsTA
ENST00000706954.1:c.973_974delinsTA	ENSP00000516674.1:p.Leu325Tyr
ENST00000706955.1:c.*1008_*1009delinsTA	ENSP00000516675.1:n.*1008_*1009delinsTA
ENST00000686459.1:c.*559_*560delinsTA	ENSP00000508909.1:n.*559_*560delinsTA
ENST00000688158.1:c.*1084_*1085delinsTA	ENSP00000509254.1:n.*1084_*1085delinsTA
ENST00000688308.1:c.973_974delinsTA	ENSP00000508752.1:p.Leu325Tyr
ENST00000688922.1:c.894_895delinsTA
ENST00000693560.1:c.1492_1493delinsTA	ENSP00000509861.1:p.Leu498Tyr
ENST00000371953.8:c.973_974delinsTA MANE Select	ENSP00000361021.3:p.Leu325Tyr
ENST00000371953.7:c.973_974delinsTA	ENSP00000361021.3:p.Leu325Tyr
ENST00000472832.2:c.400_401delinsTA	ENSP00000483066.1:p.Leu134Tyr
NM_000314.5:c.973_974delinsTA	NP_000305.3:p.Leu325Tyr
NM_000314.6:c.973_974delinsTA	NP_000305.3:p.Leu325Tyr
NM_001304717.2:c.1492_1493delinsTA	NP_001291646.2:p.Leu498Tyr
NM_001304718.1:c.382_383delinsTA	NP_001291647.1:p.Leu128Tyr
XM_006717926.2:c.928_929delinsTA	XP_006717989.1:p.Leu310Tyr
XM_011539981.1:c.973_974delinsTA	XP_011538283.1:p.Leu325Tyr
XM_011539982.1:c.877_878delinsTA	XP_011538284.1:p.Leu293Tyr
XR_945791.1:n.1543_1544delinsTA
NM_000314.7:c.973_974delinsTA	NP_000305.3:p.Leu325Tyr
NM_001304717.5:c.1492_1493delinsTA	NP_001291646.4:p.Leu498Tyr
NM_001304718.2:c.382_383delinsTA	NP_001291647.1:p.Leu128Tyr
NM_000314.8:c.973_974delinsTA MANE Select	NP_000305.3:p.Leu325Tyr