Canonical Allele Identifier: CA891839913

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957972_87957973delinsTT , CM000672.2:g.87957972_87957973delinsTT	GRCh38
NC_000010.10:g.89717729_89717730delinsTT , CM000672.1:g.89717729_89717730delinsTT	GRCh37
NC_000010.9:g.89707709_89707710delinsTT	NCBI36
NG_007466.2:g.99534_99535delinsTT , LRG_311:g.99534_99535delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.754_755delinsTT	ENSP00000514759.2:p.Asp252Phe
ENST00000710265.1:c.754_755delinsTT	ENSP00000518161.1:p.Asp252Phe
ENST00000472832.3:c.754_755delinsTT	ENSP00000483066.2:p.Asp252Phe
ENST00000688158.2:n.1489_1490delinsTT
ENST00000688922.2:c.*584_*585delinsTT	ENSP00000508742.2:n.*584_*585delinsTT
ENST00000700021.1:c.709_710delinsTT	ENSP00000514757.1:p.Asp237Phe
ENST00000700022.1:c.*93_*94delinsTT	ENSP00000514758.1:n.*93_*94delinsTT
ENST00000700023.1:n.1912_1913delinsTT
ENST00000700024.1:n.2146_2147delinsTT
ENST00000700025.1:n.1523_1524delinsTT
ENST00000700026.1:n.391_392delinsTT
ENST00000700029.1:c.588_589delinsTT
ENST00000706954.1:c.754_755delinsTT	ENSP00000516674.1:p.Asp252Phe
ENST00000706955.1:c.*789_*790delinsTT	ENSP00000516675.1:n.*789_*790delinsTT
ENST00000686459.1:c.*340_*341delinsTT	ENSP00000508909.1:n.*340_*341delinsTT
ENST00000688158.1:c.*865_*866delinsTT	ENSP00000509254.1:n.*865_*866delinsTT
ENST00000688308.1:c.754_755delinsTT	ENSP00000508752.1:p.Asp252Phe
ENST00000688922.1:c.675_676delinsTT
ENST00000693560.1:c.1273_1274delinsTT	ENSP00000509861.1:p.Asp425Phe
ENST00000371953.8:c.754_755delinsTT MANE Select	ENSP00000361021.3:p.Asp252Phe
ENST00000371953.7:c.754_755delinsTT	ENSP00000361021.3:p.Asp252Phe
ENST00000472832.2:c.181_182delinsTT	ENSP00000483066.1:p.Asp61Phe
NM_000314.5:c.754_755delinsTT	NP_000305.3:p.Asp252Phe
NM_000314.6:c.754_755delinsTT	NP_000305.3:p.Asp252Phe
NM_001304717.2:c.1273_1274delinsTT	NP_001291646.2:p.Asp425Phe
NM_001304718.1:c.163_164delinsTT	NP_001291647.1:p.Asp55Phe
XM_006717926.2:c.709_710delinsTT	XP_006717989.1:p.Asp237Phe
XM_011539981.1:c.754_755delinsTT	XP_011538283.1:p.Asp252Phe
XM_011539982.1:c.658_659delinsTT	XP_011538284.1:p.Asp220Phe
XR_945791.1:n.1324_1325delinsTT
NM_000314.7:c.754_755delinsTT	NP_000305.3:p.Asp252Phe
NM_001304717.5:c.1273_1274delinsTT	NP_001291646.4:p.Asp425Phe
NM_001304718.2:c.163_164delinsTT	NP_001291647.1:p.Asp55Phe
NM_000314.8:c.754_755delinsTT MANE Select	NP_000305.3:p.Asp252Phe