Canonical Allele Identifier: CA594924223

Gene: PTEN

Linked Data

• gnomAD v2: 10-89727265-T-TA
• gnomAD v3: 10-87967508-T-TA
• gnomAD v4: 10-87967508-T-TA
• MyVariant Identifiers: chr10:g.89727265_89727266insA (hg19) ; chr10:g.87967508_87967509insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967509dup , CM000672.2:g.87967509dup	GRCh38
NC_000010.10:g.89727266dup , CM000672.1:g.89727266dup	GRCh37
NC_000010.9:g.89717246dup	NCBI36
NG_007466.2:g.109071dup , LRG_311:g.109071dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*2278dup	ENSP00000518161.1:n.*2278dup
ENST00000688158.2:n.3984dup
ENST00000706954.1:c.*2037dup	ENSP00000516674.1:n.*2037dup
ENST00000706955.1:c.*3284dup	ENSP00000516675.1:n.*3284dup
ENST00000688158.1:c.*3360dup	ENSP00000509254.1:n.*3360dup
ENST00000693560.1:c.*2037dup	ENSP00000509861.1:n.*2037dup
ENST00000371953.8:c.*2037dup MANE Select	ENSP00000361021.3:n.*2037dup
ENST00000371953.7:c.*2037dup	ENSP00000361021.3:n.*2037dup
NM_000314.5:c.*2037dup	NP_000305.3:n.*2037dup
NM_000314.6:c.*2037dup	NP_000305.3:n.*2037dup
NM_001304717.2:c.*2037dup	NP_001291646.2:n.*2037dup
NM_001304718.1:c.*2037dup	NP_001291647.1:n.*2037dup
XM_006717926.2:c.*2037dup	XP_006717989.1:n.*2037dup
XM_011539982.1:c.*2037dup	XP_011538284.1:n.*2037dup
XR_945791.1:n.3819dup
NM_000314.7:c.*2037dup	NP_000305.3:n.*2037dup
NM_001304717.5:c.*2037dup	NP_001291646.4:n.*2037dup
NM_001304718.2:c.*2037dup	NP_001291647.1:n.*2037dup
NM_000314.8:c.*2037dup MANE Select	NP_000305.3:n.*2037dup