Canonical Allele Identifier: CA377485460

Gene: PTEN

Linked Data

• dbSNP Id: rs1860616865
• gnomAD v3: 10-87960906-C-A
• gnomAD v4: 10-87960906-C-A
• MyVariant Identifiers: chr10:g.89720663C>A (hg19) ; chr10:g.87960906C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960906C>A , CM000672.2:g.87960906C>A	GRCh38
NC_000010.10:g.89720663C>A , CM000672.1:g.89720663C>A	GRCh37
NC_000010.9:g.89710643C>A	NCBI36
NG_007466.2:g.102468C>A , LRG_311:g.102468C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.907C>A	ENSP00000514759.2:p.His303Asn
ENST00000710265.1:c.814C>A	ENSP00000518161.1:p.His272Asn
ENST00000472832.3:c.814C>A	ENSP00000483066.2:p.His272Asn
ENST00000688158.2:n.1549C>A
ENST00000688922.2:c.*644C>A	ENSP00000508742.2:n.*644C>A
ENST00000700021.1:c.769C>A	ENSP00000514757.1:p.His257Asn
ENST00000700022.1:c.*153C>A	ENSP00000514758.1:n.*153C>A
ENST00000700023.1:n.1972C>A
ENST00000700024.1:n.2206C>A
ENST00000700025.1:n.1583C>A
ENST00000700026.1:n.451C>A
ENST00000700029.1:c.741C>A
ENST00000706954.1:c.814C>A	ENSP00000516674.1:p.His272Asn
ENST00000706955.1:c.*849C>A	ENSP00000516675.1:n.*849C>A
ENST00000686459.1:c.*400C>A	ENSP00000508909.1:n.*400C>A
ENST00000688158.1:c.*925C>A	ENSP00000509254.1:n.*925C>A
ENST00000688308.1:c.814C>A	ENSP00000508752.1:p.His272Asn
ENST00000688922.1:c.735C>A
ENST00000693560.1:c.1333C>A	ENSP00000509861.1:p.His445Asn
ENST00000371953.8:c.814C>A MANE Select	ENSP00000361021.3:p.His272Asn
ENST00000371953.7:c.814C>A	ENSP00000361021.3:p.His272Asn
ENST00000472832.2:c.241C>A	ENSP00000483066.1:p.His81Asn
NM_000314.5:c.814C>A	NP_000305.3:p.His272Asn
NM_000314.6:c.814C>A	NP_000305.3:p.His272Asn
NM_001304717.2:c.1333C>A	NP_001291646.2:p.His445Asn
NM_001304718.1:c.223C>A	NP_001291647.1:p.His75Asn
XM_006717926.2:c.769C>A	XP_006717989.1:p.His257Asn
XM_011539981.1:c.814C>A	XP_011538283.1:p.His272Asn
XM_011539982.1:c.718C>A	XP_011538284.1:p.His240Asn
XR_945791.1:n.1384C>A
NM_000314.7:c.814C>A	NP_000305.3:p.His272Asn
NM_001304717.5:c.1333C>A	NP_001291646.4:p.His445Asn
NM_001304718.2:c.223C>A	NP_001291647.1:p.His75Asn
NM_000314.8:c.814C>A MANE Select	NP_000305.3:p.His272Asn