Canonical Allele Identifier: CA377485833

Gene: PTEN

Linked Data

• dbSNP Id: rs587780007
• MyVariant Identifiers: chr10:g.89720763G>C (hg19) ; chr10:g.87961006G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961006G>C , CM000672.2:g.87961006G>C	GRCh38
NC_000010.10:g.89720763G>C , CM000672.1:g.89720763G>C	GRCh37
NC_000010.9:g.89710743G>C	NCBI36
NG_007466.2:g.102568G>C , LRG_311:g.102568G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1007G>C	ENSP00000514759.2:p.Ser336Thr
ENST00000710265.1:c.914G>C	ENSP00000518161.1:p.Ser305Thr
ENST00000472832.3:c.914G>C	ENSP00000483066.2:p.Ser305Thr
ENST00000688158.2:n.1649G>C
ENST00000688922.2:c.*744G>C	ENSP00000508742.2:n.*744G>C
ENST00000700021.1:c.869G>C	ENSP00000514757.1:p.Ser290Thr
ENST00000700022.1:c.*253G>C	ENSP00000514758.1:n.*253G>C
ENST00000700023.1:n.2072G>C
ENST00000700024.1:n.2306G>C
ENST00000700025.1:n.1683G>C
ENST00000700026.1:n.551G>C
ENST00000706954.1:c.914G>C	ENSP00000516674.1:p.Ser305Thr
ENST00000706955.1:c.*949G>C	ENSP00000516675.1:n.*949G>C
ENST00000686459.1:c.*500G>C	ENSP00000508909.1:n.*500G>C
ENST00000688158.1:c.*1025G>C	ENSP00000509254.1:n.*1025G>C
ENST00000688308.1:c.914G>C	ENSP00000508752.1:p.Ser305Thr
ENST00000688922.1:c.835G>C
ENST00000693560.1:c.1433G>C	ENSP00000509861.1:p.Ser478Thr
ENST00000371953.8:c.914G>C MANE Select	ENSP00000361021.3:p.Ser305Thr
ENST00000371953.7:c.914G>C	ENSP00000361021.3:p.Ser305Thr
ENST00000472832.2:c.341G>C	ENSP00000483066.1:p.Ser114Thr
NM_000314.5:c.914G>C	NP_000305.3:p.Ser305Thr
NM_000314.6:c.914G>C	NP_000305.3:p.Ser305Thr
NM_001304717.2:c.1433G>C	NP_001291646.2:p.Ser478Thr
NM_001304718.1:c.323G>C	NP_001291647.1:p.Ser108Thr
XM_006717926.2:c.869G>C	XP_006717989.1:p.Ser290Thr
XM_011539981.1:c.914G>C	XP_011538283.1:p.Ser305Thr
XM_011539982.1:c.818G>C	XP_011538284.1:p.Ser273Thr
XR_945791.1:n.1484G>C
NM_000314.7:c.914G>C	NP_000305.3:p.Ser305Thr
NM_001304717.5:c.1433G>C	NP_001291646.4:p.Ser478Thr
NM_001304718.2:c.323G>C	NP_001291647.1:p.Ser108Thr
NM_000314.8:c.914G>C MANE Select	NP_000305.3:p.Ser305Thr