Canonical Allele Identifier: CA891839908

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957972_87957974delinsAAA , CM000672.2:g.87957972_87957974delinsAAA	GRCh38
NC_000010.10:g.89717729_89717731delinsAAA , CM000672.1:g.89717729_89717731delinsAAA	GRCh37
NC_000010.9:g.89707709_89707711delinsAAA	NCBI36
NG_007466.2:g.99534_99536delinsAAA , LRG_311:g.99534_99536delinsAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.754_756delinsAAA	ENSP00000514759.2:p.Asp252Lys
ENST00000710265.1:c.754_756delinsAAA	ENSP00000518161.1:p.Asp252Lys
ENST00000472832.3:c.754_756delinsAAA	ENSP00000483066.2:p.Asp252Lys
ENST00000688158.2:n.1489_1491delinsAAA
ENST00000688922.2:c.*584_*586delinsAAA	ENSP00000508742.2:n.*584_*586delinsAAA
ENST00000700021.1:c.709_711delinsAAA	ENSP00000514757.1:p.Asp237Lys
ENST00000700022.1:c.*93_*95delinsAAA	ENSP00000514758.1:n.*93_*95delinsAAA
ENST00000700023.1:n.1912_1914delinsAAA
ENST00000700024.1:n.2146_2148delinsAAA
ENST00000700025.1:n.1523_1525delinsAAA
ENST00000700026.1:n.391_393delinsAAA
ENST00000700029.1:c.588_590delinsAAA
ENST00000706954.1:c.754_756delinsAAA	ENSP00000516674.1:p.Asp252Lys
ENST00000706955.1:c.*789_*791delinsAAA	ENSP00000516675.1:n.*789_*791delinsAAA
ENST00000686459.1:c.*340_*342delinsAAA	ENSP00000508909.1:n.*340_*342delinsAAA
ENST00000688158.1:c.*865_*867delinsAAA	ENSP00000509254.1:n.*865_*867delinsAAA
ENST00000688308.1:c.754_756delinsAAA	ENSP00000508752.1:p.Asp252Lys
ENST00000688922.1:c.675_677delinsAAA
ENST00000693560.1:c.1273_1275delinsAAA	ENSP00000509861.1:p.Asp425Lys
ENST00000371953.8:c.754_756delinsAAA MANE Select	ENSP00000361021.3:p.Asp252Lys
ENST00000371953.7:c.754_756delinsAAA	ENSP00000361021.3:p.Asp252Lys
ENST00000472832.2:c.181_183delinsAAA	ENSP00000483066.1:p.Asp61Lys
NM_000314.5:c.754_756delinsAAA	NP_000305.3:p.Asp252Lys
NM_000314.6:c.754_756delinsAAA	NP_000305.3:p.Asp252Lys
NM_001304717.2:c.1273_1275delinsAAA	NP_001291646.2:p.Asp425Lys
NM_001304718.1:c.163_165delinsAAA	NP_001291647.1:p.Asp55Lys
XM_006717926.2:c.709_711delinsAAA	XP_006717989.1:p.Asp237Lys
XM_011539981.1:c.754_756delinsAAA	XP_011538283.1:p.Asp252Lys
XM_011539982.1:c.658_660delinsAAA	XP_011538284.1:p.Asp220Lys
XR_945791.1:n.1324_1326delinsAAA
NM_000314.7:c.754_756delinsAAA	NP_000305.3:p.Asp252Lys
NM_001304717.5:c.1273_1275delinsAAA	NP_001291646.4:p.Asp425Lys
NM_001304718.2:c.163_165delinsAAA	NP_001291647.1:p.Asp55Lys
NM_000314.8:c.754_756delinsAAA MANE Select	NP_000305.3:p.Asp252Lys