Canonical Allele Identifier: CA377487349

Gene: PTEN

Linked Data

• COSMIC: COSM5195
• MyVariant Identifiers: chr10:g.89725161A>T (hg19) ; chr10:g.87965404A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965404A>T , CM000672.2:g.87965404A>T	GRCh38
NC_000010.10:g.89725161A>T , CM000672.1:g.89725161A>T	GRCh37
NC_000010.9:g.89715141A>T	NCBI36
NG_007466.2:g.106966A>T , LRG_311:g.106966A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1237A>T	ENSP00000514759.2:p.Thr413Ser
ENST00000710265.1:c.*173A>T	ENSP00000518161.1:n.*173A>T
ENST00000688158.2:n.1879A>T
ENST00000688922.2:c.*974A>T	ENSP00000508742.2:n.*974A>T
ENST00000700021.1:c.1099A>T	ENSP00000514757.1:p.Thr367Ser
ENST00000700022.1:c.*483A>T	ENSP00000514758.1:n.*483A>T
ENST00000700023.1:n.2302A>T
ENST00000700024.1:n.2536A>T
ENST00000706954.1:c.1144A>T	ENSP00000516674.1:p.Thr382Ser
ENST00000706955.1:c.*1179A>T	ENSP00000516675.1:n.*1179A>T
ENST00000686459.1:c.*730A>T	ENSP00000508909.1:n.*730A>T
ENST00000688158.1:c.*1255A>T	ENSP00000509254.1:n.*1255A>T
ENST00000688308.1:c.1144A>T	ENSP00000508752.1:p.Thr382Ser
ENST00000688922.1:c.1065A>T
ENST00000693560.1:c.1663A>T	ENSP00000509861.1:p.Thr555Ser
ENST00000371953.8:c.1144A>T MANE Select	ENSP00000361021.3:p.Thr382Ser
ENST00000371953.7:c.1144A>T	ENSP00000361021.3:p.Thr382Ser
NM_000314.5:c.1144A>T	NP_000305.3:p.Thr382Ser
NM_000314.6:c.1144A>T	NP_000305.3:p.Thr382Ser
NM_001304717.2:c.1663A>T	NP_001291646.2:p.Thr555Ser
NM_001304718.1:c.553A>T	NP_001291647.1:p.Thr185Ser
XM_006717926.2:c.1099A>T	XP_006717989.1:p.Thr367Ser
XM_011539982.1:c.1048A>T	XP_011538284.1:p.Thr350Ser
XR_945791.1:n.1714A>T
NM_000314.7:c.1144A>T	NP_000305.3:p.Thr382Ser
NM_001304717.5:c.1663A>T	NP_001291646.4:p.Thr555Ser
NM_001304718.2:c.553A>T	NP_001291647.1:p.Thr185Ser
NM_000314.8:c.1144A>T MANE Select	NP_000305.3:p.Thr382Ser