Canonical Allele Identifier: CA2788895764

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925410_87925411insTACCTG , CM000672.2:g.87925410_87925411insTACCTG	GRCh38
NC_000010.10:g.89685167_89685168insTACCTG , CM000672.1:g.89685167_89685168insTACCTG	GRCh37
NC_000010.9:g.89675147_89675148insTACCTG	NCBI36
NG_007466.2:g.66972_66973insTACCTG , LRG_311:g.66972_66973insTACCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.165-103_165-102insTACCTG	ENSP00000514759.2:n.165-103_165-102insTACCTG
ENST00000710265.1:c.165-103_165-102insTACCTG	ENSP00000518161.1:n.165-103_165-102insTACCTG
ENST00000472832.3:c.165-103_165-102insTACCTG	ENSP00000483066.2:n.165-103_165-102insTACCTG
ENST00000688158.2:n.900-103_900-102insTACCTG
ENST00000688922.2:c.165-103_165-102insTACCTG	ENSP00000508742.2:n.165-103_165-102insTACCTG
ENST00000700021.1:c.165-5636_165-5635insTACCTG	ENSP00000514757.1:n.165-5636_165-5635insTACCTG
ENST00000700022.1:c.165-103_165-102insTACCTG	ENSP00000514758.1:n.165-103_165-102insTACCTG
ENST00000706954.1:c.165-103_165-102insTACCTG	ENSP00000516674.1:n.165-103_165-102insTACCTG
ENST00000706955.1:c.*200-103_*200-102insTACCTG	ENSP00000516675.1:n.*200-103_*200-102insTACCTG
ENST00000686459.1:c.165-103_165-102insTACCTG	ENSP00000508909.1:n.165-103_165-102insTACCTG
ENST00000688158.1:c.*276-103_*276-102insTACCTG	ENSP00000509254.1:n.*276-103_*276-102insTACCTG
ENST00000688308.1:c.165-103_165-102insTACCTG	ENSP00000508752.1:n.165-103_165-102insTACCTG
ENST00000688922.1:c.34-103_34-102insTACCTG
ENST00000693560.1:c.684-103_684-102insTACCTG	ENSP00000509861.1:n.684-103_684-102insTACCTG
ENST00000371953.8:c.165-103_165-102insTACCTG MANE Select	ENSP00000361021.3:n.165-103_165-102insTACCTG
ENST00000371953.7:c.165-103_165-102insTACCTG	ENSP00000361021.3:n.165-103_165-102insTACCTG
ENST00000610634.1:c.63-103_63-102insTACCTG	ENSP00000477517.1:n.63-103_63-102insTACCTG
NM_000314.5:c.165-103_165-102insTACCTG	NP_000305.3:n.165-103_165-102insTACCTG
NM_000314.6:c.165-103_165-102insTACCTG	NP_000305.3:n.165-103_165-102insTACCTG
NM_001304717.2:c.684-103_684-102insTACCTG	NP_001291646.2:n.684-103_684-102insTACCTG
NM_001304718.1:c.-541-5636_-541-5635insTACCTG	NP_001291647.1:n.-541-5636_-541-5635insTACCTG
XM_006717926.2:c.165-5636_165-5635insTACCTG	XP_006717989.1:n.165-5636_165-5635insTACCTG
XM_011539981.1:c.165-103_165-102insTACCTG	XP_011538283.1:n.165-103_165-102insTACCTG
XM_011539982.1:c.69-103_69-102insTACCTG	XP_011538284.1:n.69-103_69-102insTACCTG
XR_945789.1:n.877-103_877-102insTACCTG
XR_945790.1:n.877-103_877-102insTACCTG
XR_945791.1:n.877-103_877-102insTACCTG
NM_000314.7:c.165-103_165-102insTACCTG	NP_000305.3:n.165-103_165-102insTACCTG
NM_001304717.5:c.684-103_684-102insTACCTG	NP_001291646.4:n.684-103_684-102insTACCTG
NM_001304718.2:c.-541-5636_-541-5635insTACCTG	NP_001291647.1:n.-541-5636_-541-5635insTACCTG
NM_000314.8:c.165-103_165-102insTACCTG MANE Select	NP_000305.3:n.165-103_165-102insTACCTG