Canonical Allele Identifier: CA377487334

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725155T>C (hg19) ; chr10:g.87965398T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965398T>C , CM000672.2:g.87965398T>C	GRCh38
NC_000010.10:g.89725155T>C , CM000672.1:g.89725155T>C	GRCh37
NC_000010.9:g.89715135T>C	NCBI36
NG_007466.2:g.106960T>C , LRG_311:g.106960T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1231T>C	ENSP00000514759.2:p.Ser411Pro
ENST00000710265.1:c.*167T>C	ENSP00000518161.1:n.*167T>C
ENST00000688158.2:n.1873T>C
ENST00000688922.2:c.*968T>C	ENSP00000508742.2:n.*968T>C
ENST00000700021.1:c.1093T>C	ENSP00000514757.1:p.Ser365Pro
ENST00000700022.1:c.*477T>C	ENSP00000514758.1:n.*477T>C
ENST00000700023.1:n.2296T>C
ENST00000700024.1:n.2530T>C
ENST00000706954.1:c.1138T>C	ENSP00000516674.1:p.Ser380Pro
ENST00000706955.1:c.*1173T>C	ENSP00000516675.1:n.*1173T>C
ENST00000686459.1:c.*724T>C	ENSP00000508909.1:n.*724T>C
ENST00000688158.1:c.*1249T>C	ENSP00000509254.1:n.*1249T>C
ENST00000688308.1:c.1138T>C	ENSP00000508752.1:p.Ser380Pro
ENST00000688922.1:c.1059T>C
ENST00000693560.1:c.1657T>C	ENSP00000509861.1:p.Ser553Pro
ENST00000371953.8:c.1138T>C MANE Select	ENSP00000361021.3:p.Ser380Pro
ENST00000371953.7:c.1138T>C	ENSP00000361021.3:p.Ser380Pro
NM_000314.5:c.1138T>C	NP_000305.3:p.Ser380Pro
NM_000314.6:c.1138T>C	NP_000305.3:p.Ser380Pro
NM_001304717.2:c.1657T>C	NP_001291646.2:p.Ser553Pro
NM_001304718.1:c.547T>C	NP_001291647.1:p.Ser183Pro
XM_006717926.2:c.1093T>C	XP_006717989.1:p.Ser365Pro
XM_011539982.1:c.1042T>C	XP_011538284.1:p.Ser348Pro
XR_945791.1:n.1708T>C
NM_000314.7:c.1138T>C	NP_000305.3:p.Ser380Pro
NM_001304717.5:c.1657T>C	NP_001291646.4:p.Ser553Pro
NM_001304718.2:c.547T>C	NP_001291647.1:p.Ser183Pro
NM_000314.8:c.1138T>C MANE Select	NP_000305.3:p.Ser380Pro