Canonical Allele Identifier: CA891838712

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952139_87952141delinsCCA , CM000672.2:g.87952139_87952141delinsCCA	GRCh38
NC_000010.10:g.89711896_89711898delinsCCA , CM000672.1:g.89711896_89711898delinsCCA	GRCh37
NC_000010.9:g.89701876_89701878delinsCCA	NCBI36
NG_007466.2:g.93701_93703delinsCCA , LRG_311:g.93701_93703delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.514_516delinsCCA	ENSP00000514759.2:p.Arg172Pro
ENST00000710265.1:c.514_516delinsCCA	ENSP00000518161.1:p.Arg172Pro
ENST00000472832.3:c.514_516delinsCCA	ENSP00000483066.2:p.Arg172Pro
ENST00000688158.2:n.1249_1251delinsCCA
ENST00000688922.2:c.*344_*346delinsCCA	ENSP00000508742.2:n.*344_*346delinsCCA
ENST00000700021.1:c.469_471delinsCCA	ENSP00000514757.1:p.Arg157Pro
ENST00000700022.1:c.493-5714_493-5712delinsCCA	ENSP00000514758.1:n.493-5714_493-5712delinsCCA
ENST00000700023.1:n.1672_1674delinsCCA
ENST00000700024.1:n.1906_1908delinsCCA
ENST00000700025.1:n.1283_1285delinsCCA
ENST00000700029.1:c.348_350delinsCCA
ENST00000706954.1:c.514_516delinsCCA	ENSP00000516674.1:p.Arg172Pro
ENST00000706955.1:c.*549_*551delinsCCA	ENSP00000516675.1:n.*549_*551delinsCCA
ENST00000686459.1:c.*100_*102delinsCCA	ENSP00000508909.1:n.*100_*102delinsCCA
ENST00000688158.1:c.*625_*627delinsCCA	ENSP00000509254.1:n.*625_*627delinsCCA
ENST00000688308.1:c.514_516delinsCCA	ENSP00000508752.1:p.Arg172Pro
ENST00000688922.1:c.435_437delinsCCA
ENST00000693560.1:c.1033_1035delinsCCA	ENSP00000509861.1:p.Arg345Pro
ENST00000371953.8:c.514_516delinsCCA MANE Select	ENSP00000361021.3:p.Arg172Pro
ENST00000371953.7:c.514_516delinsCCA	ENSP00000361021.3:p.Arg172Pro
NM_000314.5:c.514_516delinsCCA	NP_000305.3:p.Arg172Pro
NM_000314.6:c.514_516delinsCCA	NP_000305.3:p.Arg172Pro
NM_001304717.2:c.1033_1035delinsCCA	NP_001291646.2:p.Arg345Pro
NM_001304718.1:c.-78_-76delinsCCA	NP_001291647.1:n.-78_-76delinsCCA
XM_006717926.2:c.469_471delinsCCA	XP_006717989.1:p.Arg157Pro
XM_011539981.1:c.514_516delinsCCA	XP_011538283.1:p.Arg172Pro
XM_011539982.1:c.418_420delinsCCA	XP_011538284.1:p.Arg140Pro
XR_945789.1:n.1385_1387delinsCCA
XR_945790.1:n.1502_1504delinsCCA
XR_945791.1:n.1205-5714_1205-5712delinsCCA
NM_000314.7:c.514_516delinsCCA	NP_000305.3:p.Arg172Pro
NM_001304717.5:c.1033_1035delinsCCA	NP_001291646.4:p.Arg345Pro
NM_001304718.2:c.-78_-76delinsCCA	NP_001291647.1:n.-78_-76delinsCCA
NM_000314.8:c.514_516delinsCCA MANE Select	NP_000305.3:p.Arg172Pro