Canonical Allele Identifier: CA891836516

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961044_87961046delinsATG , CM000672.2:g.87961044_87961046delinsATG	GRCh38
NC_000010.10:g.89720801_89720803delinsATG , CM000672.1:g.89720801_89720803delinsATG	GRCh37
NC_000010.9:g.89710781_89710783delinsATG	NCBI36
NG_007466.2:g.102606_102608delinsATG , LRG_311:g.102606_102608delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1045_1047delinsATG	ENSP00000514759.2:p.Leu349Met
ENST00000710265.1:c.952_954delinsATG	ENSP00000518161.1:p.Leu318Met
ENST00000472832.3:c.952_954delinsATG	ENSP00000483066.2:p.Leu318Met
ENST00000688158.2:n.1687_1689delinsATG
ENST00000688922.2:c.*782_*784delinsATG	ENSP00000508742.2:n.*782_*784delinsATG
ENST00000700021.1:c.907_909delinsATG	ENSP00000514757.1:p.Leu303Met
ENST00000700022.1:c.*291_*293delinsATG	ENSP00000514758.1:n.*291_*293delinsATG
ENST00000700023.1:n.2110_2112delinsATG
ENST00000700024.1:n.2344_2346delinsATG
ENST00000700025.1:n.1721_1723delinsATG
ENST00000700026.1:n.589_591delinsATG
ENST00000706954.1:c.952_954delinsATG	ENSP00000516674.1:p.Leu318Met
ENST00000706955.1:c.*987_*989delinsATG	ENSP00000516675.1:n.*987_*989delinsATG
ENST00000686459.1:c.*538_*540delinsATG	ENSP00000508909.1:n.*538_*540delinsATG
ENST00000688158.1:c.*1063_*1065delinsATG	ENSP00000509254.1:n.*1063_*1065delinsATG
ENST00000688308.1:c.952_954delinsATG	ENSP00000508752.1:p.Leu318Met
ENST00000688922.1:c.873_875delinsATG
ENST00000693560.1:c.1471_1473delinsATG	ENSP00000509861.1:p.Leu491Met
ENST00000371953.8:c.952_954delinsATG MANE Select	ENSP00000361021.3:p.Leu318Met
ENST00000371953.7:c.952_954delinsATG	ENSP00000361021.3:p.Leu318Met
ENST00000472832.2:c.379_381delinsATG	ENSP00000483066.1:p.Leu127Met
NM_000314.5:c.952_954delinsATG	NP_000305.3:p.Leu318Met
NM_000314.6:c.952_954delinsATG	NP_000305.3:p.Leu318Met
NM_001304717.2:c.1471_1473delinsATG	NP_001291646.2:p.Leu491Met
NM_001304718.1:c.361_363delinsATG	NP_001291647.1:p.Leu121Met
XM_006717926.2:c.907_909delinsATG	XP_006717989.1:p.Leu303Met
XM_011539981.1:c.952_954delinsATG	XP_011538283.1:p.Leu318Met
XM_011539982.1:c.856_858delinsATG	XP_011538284.1:p.Leu286Met
XR_945791.1:n.1522_1524delinsATG
NM_000314.7:c.952_954delinsATG	NP_000305.3:p.Leu318Met
NM_001304717.5:c.1471_1473delinsATG	NP_001291646.4:p.Leu491Met
NM_001304718.2:c.361_363delinsATG	NP_001291647.1:p.Leu121Met
NM_000314.8:c.952_954delinsATG MANE Select	NP_000305.3:p.Leu318Met