Canonical Allele Identifier: CA377485787

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89720751A>C (hg19) ; chr10:g.87960994A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960994A>C , CM000672.2:g.87960994A>C	GRCh38
NC_000010.10:g.89720751A>C , CM000672.1:g.89720751A>C	GRCh37
NC_000010.9:g.89710731A>C	NCBI36
NG_007466.2:g.102556A>C , LRG_311:g.102556A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.995A>C	ENSP00000514759.2:p.Asp332Ala
ENST00000710265.1:c.902A>C	ENSP00000518161.1:p.Asp301Ala
ENST00000472832.3:c.902A>C	ENSP00000483066.2:p.Asp301Ala
ENST00000688158.2:n.1637A>C
ENST00000688922.2:c.*732A>C	ENSP00000508742.2:n.*732A>C
ENST00000700021.1:c.857A>C	ENSP00000514757.1:p.Asp286Ala
ENST00000700022.1:c.*241A>C	ENSP00000514758.1:n.*241A>C
ENST00000700023.1:n.2060A>C
ENST00000700024.1:n.2294A>C
ENST00000700025.1:n.1671A>C
ENST00000700026.1:n.539A>C
ENST00000706954.1:c.902A>C	ENSP00000516674.1:p.Asp301Ala
ENST00000706955.1:c.*937A>C	ENSP00000516675.1:n.*937A>C
ENST00000686459.1:c.*488A>C	ENSP00000508909.1:n.*488A>C
ENST00000688158.1:c.*1013A>C	ENSP00000509254.1:n.*1013A>C
ENST00000688308.1:c.902A>C	ENSP00000508752.1:p.Asp301Ala
ENST00000688922.1:c.823A>C
ENST00000693560.1:c.1421A>C	ENSP00000509861.1:p.Asp474Ala
ENST00000371953.8:c.902A>C MANE Select	ENSP00000361021.3:p.Asp301Ala
ENST00000371953.7:c.902A>C	ENSP00000361021.3:p.Asp301Ala
ENST00000472832.2:c.329A>C	ENSP00000483066.1:p.Asp110Ala
NM_000314.5:c.902A>C	NP_000305.3:p.Asp301Ala
NM_000314.6:c.902A>C	NP_000305.3:p.Asp301Ala
NM_001304717.2:c.1421A>C	NP_001291646.2:p.Asp474Ala
NM_001304718.1:c.311A>C	NP_001291647.1:p.Asp104Ala
XM_006717926.2:c.857A>C	XP_006717989.1:p.Asp286Ala
XM_011539981.1:c.902A>C	XP_011538283.1:p.Asp301Ala
XM_011539982.1:c.806A>C	XP_011538284.1:p.Asp269Ala
XR_945791.1:n.1472A>C
NM_000314.7:c.902A>C	NP_000305.3:p.Asp301Ala
NM_001304717.5:c.1421A>C	NP_001291646.4:p.Asp474Ala
NM_001304718.2:c.311A>C	NP_001291647.1:p.Asp104Ala
NM_000314.8:c.902A>C MANE Select	NP_000305.3:p.Asp301Ala