Canonical Allele Identifier: CA377485809

Gene: PTEN

Linked Data

• dbSNP Id: rs772018727
• MyVariant Identifiers: chr10:g.89720757T>A (hg19) ; chr10:g.87961000T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961000T>A , CM000672.2:g.87961000T>A	GRCh38
NC_000010.10:g.89720757T>A , CM000672.1:g.89720757T>A	GRCh37
NC_000010.9:g.89710737T>A	NCBI36
NG_007466.2:g.102562T>A , LRG_311:g.102562T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1001T>A	ENSP00000514759.2:p.Ile334Asn
ENST00000710265.1:c.908T>A	ENSP00000518161.1:p.Ile303Asn
ENST00000472832.3:c.908T>A	ENSP00000483066.2:p.Ile303Asn
ENST00000688158.2:n.1643T>A
ENST00000688922.2:c.*738T>A	ENSP00000508742.2:n.*738T>A
ENST00000700021.1:c.863T>A	ENSP00000514757.1:p.Ile288Asn
ENST00000700022.1:c.*247T>A	ENSP00000514758.1:n.*247T>A
ENST00000700023.1:n.2066T>A
ENST00000700024.1:n.2300T>A
ENST00000700025.1:n.1677T>A
ENST00000700026.1:n.545T>A
ENST00000706954.1:c.908T>A	ENSP00000516674.1:p.Ile303Asn
ENST00000706955.1:c.*943T>A	ENSP00000516675.1:n.*943T>A
ENST00000686459.1:c.*494T>A	ENSP00000508909.1:n.*494T>A
ENST00000688158.1:c.*1019T>A	ENSP00000509254.1:n.*1019T>A
ENST00000688308.1:c.908T>A	ENSP00000508752.1:p.Ile303Asn
ENST00000688922.1:c.829T>A
ENST00000693560.1:c.1427T>A	ENSP00000509861.1:p.Ile476Asn
ENST00000371953.8:c.908T>A MANE Select	ENSP00000361021.3:p.Ile303Asn
ENST00000371953.7:c.908T>A	ENSP00000361021.3:p.Ile303Asn
ENST00000472832.2:c.335T>A	ENSP00000483066.1:p.Ile112Asn
NM_000314.5:c.908T>A	NP_000305.3:p.Ile303Asn
NM_000314.6:c.908T>A	NP_000305.3:p.Ile303Asn
NM_001304717.2:c.1427T>A	NP_001291646.2:p.Ile476Asn
NM_001304718.1:c.317T>A	NP_001291647.1:p.Ile106Asn
XM_006717926.2:c.863T>A	XP_006717989.1:p.Ile288Asn
XM_011539981.1:c.908T>A	XP_011538283.1:p.Ile303Asn
XM_011539982.1:c.812T>A	XP_011538284.1:p.Ile271Asn
XR_945791.1:n.1478T>A
NM_000314.7:c.908T>A	NP_000305.3:p.Ile303Asn
NM_001304717.5:c.1427T>A	NP_001291646.4:p.Ile476Asn
NM_001304718.2:c.317T>A	NP_001291647.1:p.Ile106Asn
NM_000314.8:c.908T>A MANE Select	NP_000305.3:p.Ile303Asn