Canonical Allele Identifier: CA891834570

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894033_87894035delinsATG , CM000672.2:g.87894033_87894035delinsATG	GRCh38
NC_000010.10:g.89653790_89653792delinsATG , CM000672.1:g.89653790_89653792delinsATG	GRCh37
NC_000010.9:g.89643770_89643772delinsATG	NCBI36
NG_007466.2:g.35595_35597delinsATG , LRG_311:g.35595_35597delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.88_90delinsATG	ENSP00000514759.2:p.Pro30Met
ENST00000710265.1:c.88_90delinsATG	ENSP00000518161.1:p.Pro30Met
ENST00000472832.3:c.88_90delinsATG	ENSP00000483066.2:p.Pro30Met
ENST00000688158.2:n.899+13595_899+13597delinsATG
ENST00000688922.2:c.88_90delinsATG	ENSP00000508742.2:p.Pro30Met
ENST00000700021.1:c.88_90delinsATG	ENSP00000514757.1:p.Pro30Met
ENST00000700022.1:c.88_90delinsATG	ENSP00000514758.1:p.Pro30Met
ENST00000706954.1:c.88_90delinsATG	ENSP00000516674.1:p.Pro30Met
ENST00000706955.1:c.*123_*125delinsATG	ENSP00000516675.1:n.*123_*125delinsATG
ENST00000686459.1:c.88_90delinsATG	ENSP00000508909.1:p.Pro30Met
ENST00000688158.1:c.*275+13595_*275+13597delinsATG	ENSP00000509254.1:n.*275+13595_*275+13597delinsATG
ENST00000688308.1:c.88_90delinsATG	ENSP00000508752.1:p.Pro30Met
ENST00000693560.1:c.607_609delinsATG	ENSP00000509861.1:p.Pro203Met
ENST00000371953.8:c.88_90delinsATG MANE Select	ENSP00000361021.3:p.Pro30Met
ENST00000371953.7:c.88_90delinsATG	ENSP00000361021.3:p.Pro30Met
ENST00000462694.1:n.90_92delinsATG
ENST00000610634.1:c.-15_-13delinsATG	ENSP00000477517.1:n.-15_-13delinsATG
NM_000314.5:c.88_90delinsATG	NP_000305.3:p.Pro30Met
NM_000314.6:c.88_90delinsATG	NP_000305.3:p.Pro30Met
NM_001304717.2:c.607_609delinsATG	NP_001291646.2:p.Pro203Met
NM_001304718.1:c.-618_-616delinsATG	NP_001291647.1:n.-618_-616delinsATG
XM_006717926.2:c.88_90delinsATG	XP_006717989.1:p.Pro30Met
XM_011539981.1:c.88_90delinsATG	XP_011538283.1:p.Pro30Met
XM_011539982.1:c.68+13595_68+13597delinsATG	XP_011538284.1:n.68+13595_68+13597delinsATG
XR_945789.1:n.800_802delinsATG
XR_945790.1:n.800_802delinsATG
XR_945791.1:n.800_802delinsATG
NM_000314.7:c.88_90delinsATG	NP_000305.3:p.Pro30Met
NM_001304717.5:c.607_609delinsATG	NP_001291646.4:p.Pro203Met
NM_001304718.2:c.-618_-616delinsATG	NP_001291647.1:n.-618_-616delinsATG
NM_000314.8:c.88_90delinsATG MANE Select	NP_000305.3:p.Pro30Met