Canonical Allele Identifier: CA377484311

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89711903A>C (hg19) ; chr10:g.87952146A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952146A>C , CM000672.2:g.87952146A>C	GRCh38
NC_000010.10:g.89711903A>C , CM000672.1:g.89711903A>C	GRCh37
NC_000010.9:g.89701883A>C	NCBI36
NG_007466.2:g.93708A>C , LRG_311:g.93708A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.521A>C	ENSP00000514759.2:p.Tyr174Ser
ENST00000710265.1:c.521A>C	ENSP00000518161.1:p.Tyr174Ser
ENST00000472832.3:c.521A>C	ENSP00000483066.2:p.Tyr174Ser
ENST00000688158.2:n.1256A>C
ENST00000688922.2:c.*351A>C	ENSP00000508742.2:n.*351A>C
ENST00000700021.1:c.476A>C	ENSP00000514757.1:p.Tyr159Ser
ENST00000700022.1:c.493-5707A>C	ENSP00000514758.1:n.493-5707A>C
ENST00000700023.1:n.1679A>C
ENST00000700024.1:n.1913A>C
ENST00000700025.1:n.1290A>C
ENST00000700029.1:c.355A>C
ENST00000706954.1:c.521A>C	ENSP00000516674.1:p.Tyr174Ser
ENST00000706955.1:c.*556A>C	ENSP00000516675.1:n.*556A>C
ENST00000686459.1:c.*107A>C	ENSP00000508909.1:n.*107A>C
ENST00000688158.1:c.*632A>C	ENSP00000509254.1:n.*632A>C
ENST00000688308.1:c.521A>C	ENSP00000508752.1:p.Tyr174Ser
ENST00000688922.1:c.442A>C
ENST00000693560.1:c.1040A>C	ENSP00000509861.1:p.Tyr347Ser
ENST00000371953.8:c.521A>C MANE Select	ENSP00000361021.3:p.Tyr174Ser
ENST00000371953.7:c.521A>C	ENSP00000361021.3:p.Tyr174Ser
NM_000314.5:c.521A>C	NP_000305.3:p.Tyr174Ser
NM_000314.6:c.521A>C	NP_000305.3:p.Tyr174Ser
NM_001304717.2:c.1040A>C	NP_001291646.2:p.Tyr347Ser
NM_001304718.1:c.-71A>C	NP_001291647.1:n.-71A>C
XM_006717926.2:c.476A>C	XP_006717989.1:p.Tyr159Ser
XM_011539981.1:c.521A>C	XP_011538283.1:p.Tyr174Ser
XM_011539982.1:c.425A>C	XP_011538284.1:p.Tyr142Ser
XR_945789.1:n.1392A>C
XR_945790.1:n.1509A>C
XR_945791.1:n.1205-5707A>C
NM_000314.7:c.521A>C	NP_000305.3:p.Tyr174Ser
NM_001304717.5:c.1040A>C	NP_001291646.4:p.Tyr347Ser
NM_001304718.2:c.-71A>C	NP_001291647.1:n.-71A>C
NM_000314.8:c.521A>C MANE Select	NP_000305.3:p.Tyr174Ser