Canonical Allele Identifier: CA891838707

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952137_87952138delinsCA , CM000672.2:g.87952137_87952138delinsCA	GRCh38
NC_000010.10:g.89711894_89711895delinsCA , CM000672.1:g.89711894_89711895delinsCA	GRCh37
NC_000010.9:g.89701874_89701875delinsCA	NCBI36
NG_007466.2:g.93699_93700delinsCA , LRG_311:g.93699_93700delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.512_513delinsCA	ENSP00000514759.2:p.Gln171Pro
ENST00000710265.1:c.512_513delinsCA	ENSP00000518161.1:p.Gln171Pro
ENST00000472832.3:c.512_513delinsCA	ENSP00000483066.2:p.Gln171Pro
ENST00000688158.2:n.1247_1248delinsCA
ENST00000688922.2:c.*342_*343delinsCA	ENSP00000508742.2:n.*342_*343delinsCA
ENST00000700021.1:c.467_468delinsCA	ENSP00000514757.1:p.Gln156Pro
ENST00000700022.1:c.493-5716_493-5715delinsCA	ENSP00000514758.1:n.493-5716_493-5715delinsCA
ENST00000700023.1:n.1670_1671delinsCA
ENST00000700024.1:n.1904_1905delinsCA
ENST00000700025.1:n.1281_1282delinsCA
ENST00000700029.1:c.346_347delinsCA
ENST00000706954.1:c.512_513delinsCA	ENSP00000516674.1:p.Gln171Pro
ENST00000706955.1:c.*547_*548delinsCA	ENSP00000516675.1:n.*547_*548delinsCA
ENST00000686459.1:c.*98_*99delinsCA	ENSP00000508909.1:n.*98_*99delinsCA
ENST00000688158.1:c.*623_*624delinsCA	ENSP00000509254.1:n.*623_*624delinsCA
ENST00000688308.1:c.512_513delinsCA	ENSP00000508752.1:p.Gln171Pro
ENST00000688922.1:c.433_434delinsCA
ENST00000693560.1:c.1031_1032delinsCA	ENSP00000509861.1:p.Gln344Pro
ENST00000371953.8:c.512_513delinsCA MANE Select	ENSP00000361021.3:p.Gln171Pro
ENST00000371953.7:c.512_513delinsCA	ENSP00000361021.3:p.Gln171Pro
NM_000314.5:c.512_513delinsCA	NP_000305.3:p.Gln171Pro
NM_000314.6:c.512_513delinsCA	NP_000305.3:p.Gln171Pro
NM_001304717.2:c.1031_1032delinsCA	NP_001291646.2:p.Gln344Pro
NM_001304718.1:c.-80_-79delinsCA	NP_001291647.1:n.-80_-79delinsCA
XM_006717926.2:c.467_468delinsCA	XP_006717989.1:p.Gln156Pro
XM_011539981.1:c.512_513delinsCA	XP_011538283.1:p.Gln171Pro
XM_011539982.1:c.416_417delinsCA	XP_011538284.1:p.Gln139Pro
XR_945789.1:n.1383_1384delinsCA
XR_945790.1:n.1500_1501delinsCA
XR_945791.1:n.1205-5716_1205-5715delinsCA
NM_000314.7:c.512_513delinsCA	NP_000305.3:p.Gln171Pro
NM_001304717.5:c.1031_1032delinsCA	NP_001291646.4:p.Gln344Pro
NM_001304718.2:c.-80_-79delinsCA	NP_001291647.1:n.-80_-79delinsCA
NM_000314.8:c.512_513delinsCA MANE Select	NP_000305.3:p.Gln171Pro