Canonical Allele Identifier: CA669575292

Gene: PTEN

Linked Data

• dbSNP Id: rs1224518538
• MyVariant Identifiers: chr10:g.87967985del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967985del , CM000672.2:g.87967985del	GRCh38
NC_000010.10:g.89727742del , CM000672.1:g.89727742del	GRCh37
NC_000010.9:g.89717722del	NCBI36
NG_007466.2:g.109547del , LRG_311:g.109547del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2754del	ENSP00000518161.1:n.*2754del
ENST00000688158.2:n.4460del
ENST00000706954.1:c.*2513del	ENSP00000516674.1:n.*2513del
ENST00000706955.1:c.*3760del	ENSP00000516675.1:n.*3760del
ENST00000688158.1:c.*3836del	ENSP00000509254.1:n.*3836del
ENST00000693560.1:c.*2513del	ENSP00000509861.1:n.*2513del
ENST00000371953.8:c.*2513del MANE Select	ENSP00000361021.3:n.*2513del
ENST00000371953.7:c.*2513del	ENSP00000361021.3:n.*2513del
NM_000314.5:c.*2513del	NP_000305.3:n.*2513del
NM_000314.6:c.*2513del	NP_000305.3:n.*2513del
NM_001304717.2:c.*2513del	NP_001291646.2:n.*2513del
NM_001304718.1:c.*2513del	NP_001291647.1:n.*2513del
XM_006717926.2:c.*2513del	XP_006717989.1:n.*2513del
XM_011539982.1:c.*2513del	XP_011538284.1:n.*2513del
XR_945791.1:n.4295del
NM_000314.7:c.*2513del	NP_000305.3:n.*2513del
NM_001304717.5:c.*2513del	NP_001291646.4:n.*2513del
NM_001304718.2:c.*2513del	NP_001291647.1:n.*2513del
NM_000314.8:c.*2513del MANE Select	NP_000305.3:n.*2513del