Canonical Allele Identifier: CA2580082195

Gene: PTEN

Linked Data

• ClinVar Variation Id: 1766659
• ClinVar RCV Id: RCV002450087

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863535G>A , CM000672.2:g.87863535G>A	GRCh38
NC_000010.10:g.89623292G>A , CM000672.1:g.89623292G>A	GRCh37
NC_000010.9:g.89613272G>A	NCBI36
NG_007466.2:g.5098G>A , LRG_311:g.5098G>A
NG_033079.1:g.4903C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000706954.1:c.-17+893G>A	ENSP00000516674.1:n.-17+893G>A
ENST00000688308.1:c.-17+422G>A	ENSP00000508752.1:n.-17+422G>A
ENST00000693560.1:c.-415G>A	ENSP00000509861.1:n.-415G>A
ENST00000371953.7:c.-935G>A	ENSP00000361021.3:n.-935G>A
ENST00000610634.1:c.-1037G>A	ENSP00000477517.1:n.-1037G>A
NM_000314.5:c.-934G>A	NP_000305.3:n.-934G>A
NM_000314.6:c.-934G>A	NP_000305.3:n.-934G>A
NM_001304717.2:c.-415G>A	NP_001291646.2:n.-415G>A
NM_001304718.1:c.-1639G>A	NP_001291647.1:n.-1639G>A