Canonical Allele Identifier: CA891841583

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965344_87965345delinsCG , CM000672.2:g.87965344_87965345delinsCG	GRCh38
NC_000010.10:g.89725101_89725102delinsCG , CM000672.1:g.89725101_89725102delinsCG	GRCh37
NC_000010.9:g.89715081_89715082delinsCG	NCBI36
NG_007466.2:g.106906_106907delinsCG , LRG_311:g.106906_106907delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1177_1178delinsCG	ENSP00000514759.2:p.Ser393Arg
ENST00000710265.1:c.*113_*114delinsCG	ENSP00000518161.1:n.*113_*114delinsCG
ENST00000688158.2:n.1819_1820delinsCG
ENST00000688922.2:c.*914_*915delinsCG	ENSP00000508742.2:n.*914_*915delinsCG
ENST00000700021.1:c.1039_1040delinsCG	ENSP00000514757.1:p.Ser347Arg
ENST00000700022.1:c.*423_*424delinsCG	ENSP00000514758.1:n.*423_*424delinsCG
ENST00000700023.1:n.2242_2243delinsCG
ENST00000700024.1:n.2476_2477delinsCG
ENST00000706954.1:c.1084_1085delinsCG	ENSP00000516674.1:p.Ser362Arg
ENST00000706955.1:c.*1119_*1120delinsCG	ENSP00000516675.1:n.*1119_*1120delinsCG
ENST00000686459.1:c.*670_*671delinsCG	ENSP00000508909.1:n.*670_*671delinsCG
ENST00000688158.1:c.*1195_*1196delinsCG	ENSP00000509254.1:n.*1195_*1196delinsCG
ENST00000688308.1:c.1084_1085delinsCG	ENSP00000508752.1:p.Ser362Arg
ENST00000688922.1:c.1005_1006delinsCG
ENST00000693560.1:c.1603_1604delinsCG	ENSP00000509861.1:p.Ser535Arg
ENST00000371953.8:c.1084_1085delinsCG MANE Select	ENSP00000361021.3:p.Ser362Arg
ENST00000371953.7:c.1084_1085delinsCG	ENSP00000361021.3:p.Ser362Arg
NM_000314.5:c.1084_1085delinsCG	NP_000305.3:p.Ser362Arg
NM_000314.6:c.1084_1085delinsCG	NP_000305.3:p.Ser362Arg
NM_001304717.2:c.1603_1604delinsCG	NP_001291646.2:p.Ser535Arg
NM_001304718.1:c.493_494delinsCG	NP_001291647.1:p.Ser165Arg
XM_006717926.2:c.1039_1040delinsCG	XP_006717989.1:p.Ser347Arg
XM_011539982.1:c.988_989delinsCG	XP_011538284.1:p.Ser330Arg
XR_945791.1:n.1654_1655delinsCG
NM_000314.7:c.1084_1085delinsCG	NP_000305.3:p.Ser362Arg
NM_001304717.5:c.1603_1604delinsCG	NP_001291646.4:p.Ser535Arg
NM_001304718.2:c.493_494delinsCG	NP_001291647.1:p.Ser165Arg
NM_000314.8:c.1084_1085delinsCG MANE Select	NP_000305.3:p.Ser362Arg