Canonical Allele Identifier: CA2610046365

Gene: PTEN

Linked Data

• gnomAD v4: 10-87863539-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863539G>T , CM000672.2:g.87863539G>T	GRCh38
NC_000010.10:g.89623296G>T , CM000672.1:g.89623296G>T	GRCh37
NC_000010.9:g.89613276G>T	NCBI36
NG_007466.2:g.5102G>T , LRG_311:g.5102G>T
NG_033079.1:g.4899C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000706954.1:c.-17+897G>T	ENSP00000516674.1:n.-17+897G>T
ENST00000688308.1:c.-17+426G>T	ENSP00000508752.1:n.-17+426G>T
ENST00000693560.1:c.-411G>T	ENSP00000509861.1:n.-411G>T
ENST00000371953.7:c.-931G>T	ENSP00000361021.3:n.-931G>T
ENST00000610634.1:c.-1033G>T	ENSP00000477517.1:n.-1033G>T
NM_000314.5:c.-930G>T	NP_000305.3:n.-930G>T
NM_000314.6:c.-930G>T	NP_000305.3:n.-930G>T
NM_001304717.2:c.-411G>T	NP_001291646.2:n.-411G>T
NM_001304718.1:c.-1635G>T	NP_001291647.1:n.-1635G>T