Canonical Allele Identifier: CA891838742

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952143_87952144delinsCA , CM000672.2:g.87952143_87952144delinsCA	GRCh38
NC_000010.10:g.89711900_89711901delinsCA , CM000672.1:g.89711900_89711901delinsCA	GRCh37
NC_000010.9:g.89701880_89701881delinsCA	NCBI36
NG_007466.2:g.93705_93706delinsCA , LRG_311:g.93705_93706delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.518_519delinsCA	ENSP00000514759.2:p.Arg173Pro
ENST00000710265.1:c.518_519delinsCA	ENSP00000518161.1:p.Arg173Pro
ENST00000472832.3:c.518_519delinsCA	ENSP00000483066.2:p.Arg173Pro
ENST00000688158.2:n.1253_1254delinsCA
ENST00000688922.2:c.*348_*349delinsCA	ENSP00000508742.2:n.*348_*349delinsCA
ENST00000700021.1:c.473_474delinsCA	ENSP00000514757.1:p.Arg158Pro
ENST00000700022.1:c.493-5710_493-5709delinsCA	ENSP00000514758.1:n.493-5710_493-5709delinsCA
ENST00000700023.1:n.1676_1677delinsCA
ENST00000700024.1:n.1910_1911delinsCA
ENST00000700025.1:n.1287_1288delinsCA
ENST00000700029.1:c.352_353delinsCA
ENST00000706954.1:c.518_519delinsCA	ENSP00000516674.1:p.Arg173Pro
ENST00000706955.1:c.*553_*554delinsCA	ENSP00000516675.1:n.*553_*554delinsCA
ENST00000686459.1:c.*104_*105delinsCA	ENSP00000508909.1:n.*104_*105delinsCA
ENST00000688158.1:c.*629_*630delinsCA	ENSP00000509254.1:n.*629_*630delinsCA
ENST00000688308.1:c.518_519delinsCA	ENSP00000508752.1:p.Arg173Pro
ENST00000688922.1:c.439_440delinsCA
ENST00000693560.1:c.1037_1038delinsCA	ENSP00000509861.1:p.Arg346Pro
ENST00000371953.8:c.518_519delinsCA MANE Select	ENSP00000361021.3:p.Arg173Pro
ENST00000371953.7:c.518_519delinsCA	ENSP00000361021.3:p.Arg173Pro
NM_000314.5:c.518_519delinsCA	NP_000305.3:p.Arg173Pro
NM_000314.6:c.518_519delinsCA	NP_000305.3:p.Arg173Pro
NM_001304717.2:c.1037_1038delinsCA	NP_001291646.2:p.Arg346Pro
NM_001304718.1:c.-74_-73delinsCA	NP_001291647.1:n.-74_-73delinsCA
XM_006717926.2:c.473_474delinsCA	XP_006717989.1:p.Arg158Pro
XM_011539981.1:c.518_519delinsCA	XP_011538283.1:p.Arg173Pro
XM_011539982.1:c.422_423delinsCA	XP_011538284.1:p.Arg141Pro
XR_945789.1:n.1389_1390delinsCA
XR_945790.1:n.1506_1507delinsCA
XR_945791.1:n.1205-5710_1205-5709delinsCA
NM_000314.7:c.518_519delinsCA	NP_000305.3:p.Arg173Pro
NM_001304717.5:c.1037_1038delinsCA	NP_001291646.4:p.Arg346Pro
NM_001304718.2:c.-74_-73delinsCA	NP_001291647.1:n.-74_-73delinsCA
NM_000314.8:c.518_519delinsCA MANE Select	NP_000305.3:p.Arg173Pro