Canonical Allele Identifier: CA470974034

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89720797A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961040A>C , CM000672.2:g.87961040A>C	GRCh38
NC_000010.10:g.89720797A>C , CM000672.1:g.89720797A>C	GRCh37
NC_000010.9:g.89710777A>C	NCBI36
NG_007466.2:g.102602A>C , LRG_311:g.102602A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1041A>C	ENSP00000514759.2:p.Leu347=
ENST00000710265.1:c.948A>C	ENSP00000518161.1:p.Leu316=
ENST00000472832.3:c.948A>C	ENSP00000483066.2:p.Leu316=
ENST00000688158.2:n.1683A>C
ENST00000688922.2:c.*778A>C	ENSP00000508742.2:n.*778A>C
ENST00000700021.1:c.903A>C	ENSP00000514757.1:p.Leu301=
ENST00000700022.1:c.*287A>C	ENSP00000514758.1:n.*287A>C
ENST00000700023.1:n.2106A>C
ENST00000700024.1:n.2340A>C
ENST00000700025.1:n.1717A>C
ENST00000700026.1:n.585A>C
ENST00000706954.1:c.948A>C	ENSP00000516674.1:p.Leu316=
ENST00000706955.1:c.*983A>C	ENSP00000516675.1:n.*983A>C
ENST00000686459.1:c.*534A>C	ENSP00000508909.1:n.*534A>C
ENST00000688158.1:c.*1059A>C	ENSP00000509254.1:n.*1059A>C
ENST00000688308.1:c.948A>C	ENSP00000508752.1:p.Leu316=
ENST00000688922.1:c.869A>C
ENST00000693560.1:c.1467A>C	ENSP00000509861.1:p.Leu489=
ENST00000371953.8:c.948A>C MANE Select	ENSP00000361021.3:p.Leu316=
ENST00000371953.7:c.948A>C	ENSP00000361021.3:p.Leu316=
ENST00000472832.2:c.375A>C	ENSP00000483066.1:p.Leu125=
NM_000314.5:c.948A>C	NP_000305.3:p.Leu316=
NM_000314.6:c.948A>C	NP_000305.3:p.Leu316=
NM_001304717.2:c.1467A>C	NP_001291646.2:p.Leu489=
NM_001304718.1:c.357A>C	NP_001291647.1:p.Leu119=
XM_006717926.2:c.903A>C	XP_006717989.1:p.Leu301=
XM_011539981.1:c.948A>C	XP_011538283.1:p.Leu316=
XM_011539982.1:c.852A>C	XP_011538284.1:p.Leu284=
XR_945791.1:n.1518A>C
NM_000314.7:c.948A>C	NP_000305.3:p.Leu316=
NM_001304717.5:c.1467A>C	NP_001291646.4:p.Leu489=
NM_001304718.2:c.357A>C	NP_001291647.1:p.Leu119=
NM_000314.8:c.948A>C MANE Select	NP_000305.3:p.Leu316=