Canonical Allele Identifier: CA377487496

Gene: PTEN

Linked Data

• dbSNP Id: rs2132290414
• MyVariant Identifiers: chr10:g.89725224G>C (hg19) ; chr10:g.87965467G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965467G>C , CM000672.2:g.87965467G>C	GRCh38
NC_000010.10:g.89725224G>C , CM000672.1:g.89725224G>C	GRCh37
NC_000010.9:g.89715204G>C	NCBI36
NG_007466.2:g.107029G>C , LRG_311:g.107029G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1300G>C	ENSP00000514759.2:p.Val434Leu
ENST00000710265.1:c.*236G>C	ENSP00000518161.1:n.*236G>C
ENST00000688158.2:n.1942G>C
ENST00000688922.2:c.*1037G>C	ENSP00000508742.2:n.*1037G>C
ENST00000700021.1:c.1162G>C	ENSP00000514757.1:p.Val388Leu
ENST00000700022.1:c.*546G>C	ENSP00000514758.1:n.*546G>C
ENST00000700023.1:n.2365G>C
ENST00000700024.1:n.2599G>C
ENST00000706954.1:c.1207G>C	ENSP00000516674.1:p.Val403Leu
ENST00000706955.1:c.*1242G>C	ENSP00000516675.1:n.*1242G>C
ENST00000686459.1:c.*793G>C	ENSP00000508909.1:n.*793G>C
ENST00000688158.1:c.*1318G>C	ENSP00000509254.1:n.*1318G>C
ENST00000688308.1:c.1207G>C	ENSP00000508752.1:p.Val403Leu
ENST00000688922.1:c.1128G>C
ENST00000693560.1:c.1726G>C	ENSP00000509861.1:p.Val576Leu
ENST00000371953.8:c.1207G>C MANE Select	ENSP00000361021.3:p.Val403Leu
ENST00000371953.7:c.1207G>C	ENSP00000361021.3:p.Val403Leu
NM_000314.5:c.1207G>C	NP_000305.3:p.Val403Leu
NM_000314.6:c.1207G>C	NP_000305.3:p.Val403Leu
NM_001304717.2:c.1726G>C	NP_001291646.2:p.Val576Leu
NM_001304718.1:c.616G>C	NP_001291647.1:p.Val206Leu
XM_006717926.2:c.1162G>C	XP_006717989.1:p.Val388Leu
XM_011539982.1:c.1111G>C	XP_011538284.1:p.Val371Leu
XR_945791.1:n.1777G>C
NM_000314.7:c.1207G>C	NP_000305.3:p.Val403Leu
NM_001304717.5:c.1726G>C	NP_001291646.4:p.Val576Leu
NM_001304718.2:c.616G>C	NP_001291647.1:p.Val206Leu
NM_000314.8:c.1207G>C MANE Select	NP_000305.3:p.Val403Leu