Canonical Allele Identifier: CA377486106

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89720844A>C (hg19) ; chr10:g.87961087A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961087A>C , CM000672.2:g.87961087A>C	GRCh38
NC_000010.10:g.89720844A>C , CM000672.1:g.89720844A>C	GRCh37
NC_000010.9:g.89710824A>C	NCBI36
NG_007466.2:g.102649A>C , LRG_311:g.102649A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1088A>C	ENSP00000514759.2:p.Lys363Thr
ENST00000710265.1:c.995A>C	ENSP00000518161.1:p.Lys332Thr
ENST00000472832.3:c.995A>C	ENSP00000483066.2:p.Lys332Thr
ENST00000688158.2:n.1730A>C
ENST00000688922.2:c.*825A>C	ENSP00000508742.2:n.*825A>C
ENST00000700021.1:c.950A>C	ENSP00000514757.1:p.Lys317Thr
ENST00000700022.1:c.*334A>C	ENSP00000514758.1:n.*334A>C
ENST00000700023.1:n.2153A>C
ENST00000700024.1:n.2387A>C
ENST00000700025.1:n.1764A>C
ENST00000700026.1:n.632A>C
ENST00000706954.1:c.995A>C	ENSP00000516674.1:p.Lys332Thr
ENST00000706955.1:c.*1030A>C	ENSP00000516675.1:n.*1030A>C
ENST00000686459.1:c.*581A>C	ENSP00000508909.1:n.*581A>C
ENST00000688158.1:c.*1106A>C	ENSP00000509254.1:n.*1106A>C
ENST00000688308.1:c.995A>C	ENSP00000508752.1:p.Lys332Thr
ENST00000688922.1:c.916A>C
ENST00000693560.1:c.1514A>C	ENSP00000509861.1:p.Lys505Thr
ENST00000371953.8:c.995A>C MANE Select	ENSP00000361021.3:p.Lys332Thr
ENST00000371953.7:c.995A>C	ENSP00000361021.3:p.Lys332Thr
ENST00000472832.2:c.422A>C	ENSP00000483066.1:p.Lys141Thr
NM_000314.5:c.995A>C	NP_000305.3:p.Lys332Thr
NM_000314.6:c.995A>C	NP_000305.3:p.Lys332Thr
NM_001304717.2:c.1514A>C	NP_001291646.2:p.Lys505Thr
NM_001304718.1:c.404A>C	NP_001291647.1:p.Lys135Thr
XM_006717926.2:c.950A>C	XP_006717989.1:p.Lys317Thr
XM_011539981.1:c.995A>C	XP_011538283.1:p.Lys332Thr
XM_011539982.1:c.899A>C	XP_011538284.1:p.Lys300Thr
XR_945791.1:n.1565A>C
NM_000314.7:c.995A>C	NP_000305.3:p.Lys332Thr
NM_001304717.5:c.1514A>C	NP_001291646.4:p.Lys505Thr
NM_001304718.2:c.404A>C	NP_001291647.1:p.Lys135Thr
NM_000314.8:c.995A>C MANE Select	NP_000305.3:p.Lys332Thr