Canonical Allele Identifier: CA377486086

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89720836T>G (hg19) ; chr10:g.87961079T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961079T>G , CM000672.2:g.87961079T>G	GRCh38
NC_000010.10:g.89720836T>G , CM000672.1:g.89720836T>G	GRCh37
NC_000010.9:g.89710816T>G	NCBI36
NG_007466.2:g.102641T>G , LRG_311:g.102641T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1080T>G	ENSP00000514759.2:p.Asn360Lys
ENST00000710265.1:c.987T>G	ENSP00000518161.1:p.Asn329Lys
ENST00000472832.3:c.987T>G	ENSP00000483066.2:p.Asn329Lys
ENST00000688158.2:n.1722T>G
ENST00000688922.2:c.*817T>G	ENSP00000508742.2:n.*817T>G
ENST00000700021.1:c.942T>G	ENSP00000514757.1:p.Asn314Lys
ENST00000700022.1:c.*326T>G	ENSP00000514758.1:n.*326T>G
ENST00000700023.1:n.2145T>G
ENST00000700024.1:n.2379T>G
ENST00000700025.1:n.1756T>G
ENST00000700026.1:n.624T>G
ENST00000706954.1:c.987T>G	ENSP00000516674.1:p.Asn329Lys
ENST00000706955.1:c.*1022T>G	ENSP00000516675.1:n.*1022T>G
ENST00000686459.1:c.*573T>G	ENSP00000508909.1:n.*573T>G
ENST00000688158.1:c.*1098T>G	ENSP00000509254.1:n.*1098T>G
ENST00000688308.1:c.987T>G	ENSP00000508752.1:p.Asn329Lys
ENST00000688922.1:c.908T>G
ENST00000693560.1:c.1506T>G	ENSP00000509861.1:p.Asn502Lys
ENST00000371953.8:c.987T>G MANE Select	ENSP00000361021.3:p.Asn329Lys
ENST00000371953.7:c.987T>G	ENSP00000361021.3:p.Asn329Lys
ENST00000472832.2:c.414T>G	ENSP00000483066.1:p.Asn138Lys
NM_000314.5:c.987T>G	NP_000305.3:p.Asn329Lys
NM_000314.6:c.987T>G	NP_000305.3:p.Asn329Lys
NM_001304717.2:c.1506T>G	NP_001291646.2:p.Asn502Lys
NM_001304718.1:c.396T>G	NP_001291647.1:p.Asn132Lys
XM_006717926.2:c.942T>G	XP_006717989.1:p.Asn314Lys
XM_011539981.1:c.987T>G	XP_011538283.1:p.Asn329Lys
XM_011539982.1:c.891T>G	XP_011538284.1:p.Asn297Lys
XR_945791.1:n.1557T>G
NM_000314.7:c.987T>G	NP_000305.3:p.Asn329Lys
NM_001304717.5:c.1506T>G	NP_001291646.4:p.Asn502Lys
NM_001304718.2:c.396T>G	NP_001291647.1:p.Asn132Lys
NM_000314.8:c.987T>G MANE Select	NP_000305.3:p.Asn329Lys