Canonical Allele Identifier: CA377487375

Gene: PTEN

Linked Data

• dbSNP Id: rs2132290097
• MyVariant Identifiers: chr10:g.89725173G>C (hg19) ; chr10:g.87965416G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965416G>C , CM000672.2:g.87965416G>C	GRCh38
NC_000010.10:g.89725173G>C , CM000672.1:g.89725173G>C	GRCh37
NC_000010.9:g.89715153G>C	NCBI36
NG_007466.2:g.106978G>C , LRG_311:g.106978G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1249G>C	ENSP00000514759.2:p.Asp417His
ENST00000710265.1:c.*185G>C	ENSP00000518161.1:n.*185G>C
ENST00000688158.2:n.1891G>C
ENST00000688922.2:c.*986G>C	ENSP00000508742.2:n.*986G>C
ENST00000700021.1:c.1111G>C	ENSP00000514757.1:p.Asp371His
ENST00000700022.1:c.*495G>C	ENSP00000514758.1:n.*495G>C
ENST00000700023.1:n.2314G>C
ENST00000700024.1:n.2548G>C
ENST00000706954.1:c.1156G>C	ENSP00000516674.1:p.Asp386His
ENST00000706955.1:c.*1191G>C	ENSP00000516675.1:n.*1191G>C
ENST00000686459.1:c.*742G>C	ENSP00000508909.1:n.*742G>C
ENST00000688158.1:c.*1267G>C	ENSP00000509254.1:n.*1267G>C
ENST00000688308.1:c.1156G>C	ENSP00000508752.1:p.Asp386His
ENST00000688922.1:c.1077G>C
ENST00000693560.1:c.1675G>C	ENSP00000509861.1:p.Asp559His
ENST00000371953.8:c.1156G>C MANE Select	ENSP00000361021.3:p.Asp386His
ENST00000371953.7:c.1156G>C	ENSP00000361021.3:p.Asp386His
NM_000314.5:c.1156G>C	NP_000305.3:p.Asp386His
NM_000314.6:c.1156G>C	NP_000305.3:p.Asp386His
NM_001304717.2:c.1675G>C	NP_001291646.2:p.Asp559His
NM_001304718.1:c.565G>C	NP_001291647.1:p.Asp189His
XM_006717926.2:c.1111G>C	XP_006717989.1:p.Asp371His
XM_011539982.1:c.1060G>C	XP_011538284.1:p.Asp354His
XR_945791.1:n.1726G>C
NM_000314.7:c.1156G>C	NP_000305.3:p.Asp386His
NM_001304717.5:c.1675G>C	NP_001291646.4:p.Asp559His
NM_001304718.2:c.565G>C	NP_001291647.1:p.Asp189His
NM_000314.8:c.1156G>C MANE Select	NP_000305.3:p.Asp386His