Canonical Allele Identifier: CA470882590

Gene: PTEN

Linked Data

• gnomAD v4: 10-87925519-G-A
• MyVariant Identifiers: chr10:g.89685276G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925519G>A , CM000672.2:g.87925519G>A	GRCh38
NC_000010.10:g.89685276G>A , CM000672.1:g.89685276G>A	GRCh37
NC_000010.9:g.89675256G>A	NCBI36
NG_007466.2:g.67081G>A , LRG_311:g.67081G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.171G>A	ENSP00000514759.2:p.Leu57=
ENST00000710265.1:c.171G>A	ENSP00000518161.1:p.Leu57=
ENST00000472832.3:c.171G>A	ENSP00000483066.2:p.Leu57=
ENST00000688158.2:n.906G>A
ENST00000688922.2:c.171G>A	ENSP00000508742.2:p.Leu57=
ENST00000700021.1:c.165-5527G>A	ENSP00000514757.1:n.165-5527G>A
ENST00000700022.1:c.171G>A	ENSP00000514758.1:p.Leu57=
ENST00000700029.1:c.5G>A
ENST00000706954.1:c.171G>A	ENSP00000516674.1:p.Leu57=
ENST00000706955.1:c.*206G>A	ENSP00000516675.1:n.*206G>A
ENST00000686459.1:c.171G>A	ENSP00000508909.1:p.Leu57=
ENST00000688158.1:c.*282G>A	ENSP00000509254.1:n.*282G>A
ENST00000688308.1:c.171G>A	ENSP00000508752.1:p.Leu57=
ENST00000688922.1:c.40G>A
ENST00000693560.1:c.690G>A	ENSP00000509861.1:p.Leu230=
ENST00000371953.8:c.171G>A MANE Select	ENSP00000361021.3:p.Leu57=
ENST00000371953.7:c.171G>A	ENSP00000361021.3:p.Leu57=
ENST00000610634.1:c.69G>A	ENSP00000477517.1:p.Leu23=
NM_000314.5:c.171G>A	NP_000305.3:p.Leu57=
NM_000314.6:c.171G>A	NP_000305.3:p.Leu57=
NM_001304717.2:c.690G>A	NP_001291646.2:p.Leu230=
NM_001304718.1:c.-541-5527G>A	NP_001291647.1:n.-541-5527G>A
XM_006717926.2:c.165-5527G>A	XP_006717989.1:n.165-5527G>A
XM_011539981.1:c.171G>A	XP_011538283.1:p.Leu57=
XM_011539982.1:c.75G>A	XP_011538284.1:p.Leu25=
XR_945789.1:n.883G>A
XR_945790.1:n.883G>A
XR_945791.1:n.883G>A
NM_000314.7:c.171G>A	NP_000305.3:p.Leu57=
NM_001304717.5:c.690G>A	NP_001291646.4:p.Leu230=
NM_001304718.2:c.-541-5527G>A	NP_001291647.1:n.-541-5527G>A
NM_000314.8:c.171G>A MANE Select	NP_000305.3:p.Leu57=