Canonical Allele Identifier: CA669540567

Gene: PTEN

Linked Data

• dbSNP Id: rs1471356144
• gnomAD v3: 10-87863543-A-AGGCCGGCGGGCG
• gnomAD v4: 10-87863543-A-AGGCCGGCGGGCG
• MyVariant Identifiers: chr10:g.89623300_89623301insGGCCGGCGGGCG (hg19) ; chr10:g.87863543_87863544insGGCCGGCGGGCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863545_87863556dup , CM000672.2:g.87863545_87863556dup	GRCh38
NC_000010.10:g.89623302_89623313dup , CM000672.1:g.89623302_89623313dup	GRCh37
NC_000010.9:g.89613282_89613293dup	NCBI36
NG_007466.2:g.5108_5119dup , LRG_311:g.5108_5119dup
NG_033079.1:g.4883_4894dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000706954.1:c.-17+903_-16-898dup	ENSP00000516674.1:n.-17+903_-16-898dup
ENST00000688308.1:c.-17+432_-17+443dup	ENSP00000508752.1:n.-17+432_-17+443dup
ENST00000693560.1:c.-405_-394dup	ENSP00000509861.1:n.-405_-394dup
ENST00000371953.7:c.-925_-914dup	ENSP00000361021.3:n.-925_-914dup
ENST00000610634.1:c.-1027_-1016dup	ENSP00000477517.1:n.-1027_-1016dup
NM_000314.5:c.-924_-913dup	NP_000305.3:n.-924_-913dup
NM_000314.6:c.-924_-913dup	NP_000305.3:n.-924_-913dup
NM_001304717.2:c.-405_-394dup	NP_001291646.2:n.-405_-394dup
NM_001304718.1:c.-1629_-1618dup	NP_001291647.1:n.-1629_-1618dup