Canonical Allele Identifier: CA1926176081

Gene: PTEN

Linked Data

• dbSNP Id: rs1860785549
• gnomAD v4: 10-87967013-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967013C>A , CM000672.2:g.87967013C>A	GRCh38
NC_000010.10:g.89726770C>A , CM000672.1:g.89726770C>A	GRCh37
NC_000010.9:g.89716750C>A	NCBI36
NG_007466.2:g.108575C>A , LRG_311:g.108575C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*1782C>A	ENSP00000518161.1:n.*1782C>A
ENST00000688158.2:n.3488C>A
ENST00000706954.1:c.*1541C>A	ENSP00000516674.1:n.*1541C>A
ENST00000706955.1:c.*2788C>A	ENSP00000516675.1:n.*2788C>A
ENST00000688158.1:c.*2864C>A	ENSP00000509254.1:n.*2864C>A
ENST00000693560.1:c.*1541C>A	ENSP00000509861.1:n.*1541C>A
ENST00000371953.8:c.*1541C>A MANE Select	ENSP00000361021.3:n.*1541C>A
ENST00000371953.7:c.*1541C>A	ENSP00000361021.3:n.*1541C>A
NM_000314.5:c.*1541C>A	NP_000305.3:n.*1541C>A
NM_000314.6:c.*1541C>A	NP_000305.3:n.*1541C>A
NM_001304717.2:c.*1541C>A	NP_001291646.2:n.*1541C>A
NM_001304718.1:c.*1541C>A	NP_001291647.1:n.*1541C>A
XM_006717926.2:c.*1541C>A	XP_006717989.1:n.*1541C>A
XM_011539982.1:c.*1541C>A	XP_011538284.1:n.*1541C>A
XR_945791.1:n.3323C>A
NM_000314.7:c.*1541C>A	NP_000305.3:n.*1541C>A
NM_001304717.5:c.*1541C>A	NP_001291646.4:n.*1541C>A
NM_001304718.2:c.*1541C>A	NP_001291647.1:n.*1541C>A
NM_000314.8:c.*1541C>A MANE Select	NP_000305.3:n.*1541C>A