Canonical Allele Identifier: CA2610046366

Gene: PTEN

Linked Data

• gnomAD v4: 10-87863540-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863540G>T , CM000672.2:g.87863540G>T	GRCh38
NC_000010.10:g.89623297G>T , CM000672.1:g.89623297G>T	GRCh37
NC_000010.9:g.89613277G>T	NCBI36
NG_007466.2:g.5103G>T , LRG_311:g.5103G>T
NG_033079.1:g.4898C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000706954.1:c.-17+898G>T	ENSP00000516674.1:n.-17+898G>T
ENST00000688308.1:c.-17+427G>T	ENSP00000508752.1:n.-17+427G>T
ENST00000693560.1:c.-410G>T	ENSP00000509861.1:n.-410G>T
ENST00000371953.7:c.-930G>T	ENSP00000361021.3:n.-930G>T
ENST00000610634.1:c.-1032G>T	ENSP00000477517.1:n.-1032G>T
NM_000314.5:c.-929G>T	NP_000305.3:n.-929G>T
NM_000314.6:c.-929G>T	NP_000305.3:n.-929G>T
NM_001304717.2:c.-410G>T	NP_001291646.2:n.-410G>T
NM_001304718.1:c.-1634G>T	NP_001291647.1:n.-1634G>T