Canonical Allele Identifier: CA2610049198

Gene: PTEN

Linked Data

• gnomAD v4: 10-87965485-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965486_87965487del , CM000672.2:g.87965486_87965487del	GRCh38
NC_000010.10:g.89725243_89725244del , CM000672.1:g.89725243_89725244del	GRCh37
NC_000010.9:g.89715223_89715224del	NCBI36
NG_007466.2:g.107048_107049del , LRG_311:g.107048_107049del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*14_*15del	ENSP00000514759.2:n.*14_*15del
ENST00000710265.1:c.*255_*256del	ENSP00000518161.1:n.*255_*256del
ENST00000688158.2:n.1961_1962del
ENST00000688922.2:c.*1056_*1057del	ENSP00000508742.2:n.*1056_*1057del
ENST00000700021.1:c.*14_*15del	ENSP00000514757.1:n.*14_*15del
ENST00000700022.1:c.*565_*566del	ENSP00000514758.1:n.*565_*566del
ENST00000700023.1:n.2384_2385del
ENST00000700024.1:n.2618_2619del
ENST00000706954.1:c.*14_*15del	ENSP00000516674.1:n.*14_*15del
ENST00000706955.1:c.*1261_*1262del	ENSP00000516675.1:n.*1261_*1262del
ENST00000686459.1:c.*812_*813del	ENSP00000508909.1:n.*812_*813del
ENST00000688158.1:c.*1337_*1338del	ENSP00000509254.1:n.*1337_*1338del
ENST00000688308.1:c.*14_*15del	ENSP00000508752.1:n.*14_*15del
ENST00000688922.1:c.1147_1148del
ENST00000693560.1:c.*14_*15del	ENSP00000509861.1:n.*14_*15del
ENST00000371953.8:c.*14_*15del MANE Select	ENSP00000361021.3:n.*14_*15del
ENST00000371953.7:c.*14_*15del	ENSP00000361021.3:n.*14_*15del
NM_000314.5:c.*14_*15del	NP_000305.3:n.*14_*15del
NM_000314.6:c.*14_*15del	NP_000305.3:n.*14_*15del
NM_001304717.2:c.*14_*15del	NP_001291646.2:n.*14_*15del
NM_001304718.1:c.*14_*15del	NP_001291647.1:n.*14_*15del
XM_006717926.2:c.*14_*15del	XP_006717989.1:n.*14_*15del
XM_011539982.1:c.*14_*15del	XP_011538284.1:n.*14_*15del
XR_945791.1:n.1796_1797del
NM_000314.7:c.*14_*15del	NP_000305.3:n.*14_*15del
NM_001304717.5:c.*14_*15del	NP_001291646.4:n.*14_*15del
NM_001304718.2:c.*14_*15del	NP_001291647.1:n.*14_*15del
NM_000314.8:c.*14_*15del MANE Select	NP_000305.3:n.*14_*15del