Canonical Allele Identifier: CA2610050037

Gene: PTEN

Linked Data

• gnomAD v4: 10-87967826-TGTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967829_87967831del , CM000672.2:g.87967829_87967831del	GRCh38
NC_000010.10:g.89727586_89727588del , CM000672.1:g.89727586_89727588del	GRCh37
NC_000010.9:g.89717566_89717568del	NCBI36
NG_007466.2:g.109391_109393del , LRG_311:g.109391_109393del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2598_*2600del	ENSP00000518161.1:n.*2598_*2600del
ENST00000688158.2:n.4304_4306del
ENST00000706954.1:c.*2357_*2359del	ENSP00000516674.1:n.*2357_*2359del
ENST00000706955.1:c.*3604_*3606del	ENSP00000516675.1:n.*3604_*3606del
ENST00000688158.1:c.*3680_*3682del	ENSP00000509254.1:n.*3680_*3682del
ENST00000693560.1:c.*2357_*2359del	ENSP00000509861.1:n.*2357_*2359del
ENST00000371953.8:c.*2357_*2359del MANE Select	ENSP00000361021.3:n.*2357_*2359del
ENST00000371953.7:c.*2357_*2359del	ENSP00000361021.3:n.*2357_*2359del
NM_000314.5:c.*2357_*2359del	NP_000305.3:n.*2357_*2359del
NM_000314.6:c.*2357_*2359del	NP_000305.3:n.*2357_*2359del
NM_001304717.2:c.*2357_*2359del	NP_001291646.2:n.*2357_*2359del
NM_001304718.1:c.*2357_*2359del	NP_001291647.1:n.*2357_*2359del
XM_006717926.2:c.*2357_*2359del	XP_006717989.1:n.*2357_*2359del
XM_011539982.1:c.*2357_*2359del	XP_011538284.1:n.*2357_*2359del
XR_945791.1:n.4139_4141del
NM_000314.7:c.*2357_*2359del	NP_000305.3:n.*2357_*2359del
NM_001304717.5:c.*2357_*2359del	NP_001291646.4:n.*2357_*2359del
NM_001304718.2:c.*2357_*2359del	NP_001291647.1:n.*2357_*2359del
NM_000314.8:c.*2357_*2359del MANE Select	NP_000305.3:n.*2357_*2359del