Canonical Allele Identifier: CA2513208947

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87968031_87968032insTT , CM000672.2:g.87968031_87968032insTT	GRCh38
NC_000010.10:g.89727788_89727789insTT , CM000672.1:g.89727788_89727789insTT	GRCh37
NC_000010.9:g.89717768_89717769insTT	NCBI36
NG_007466.2:g.109593_109594insTT , LRG_311:g.109593_109594insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2800_*2801insTT	ENSP00000518161.1:n.*2800_*2801insTT
ENST00000688158.2:n.4506_4507insTT
ENST00000706954.1:c.*2559_*2560insTT	ENSP00000516674.1:n.*2559_*2560insTT
ENST00000706955.1:c.*3806_*3807insTT	ENSP00000516675.1:n.*3806_*3807insTT
ENST00000688158.1:c.*3882_*3883insTT	ENSP00000509254.1:n.*3882_*3883insTT
ENST00000693560.1:c.*2559_*2560insTT	ENSP00000509861.1:n.*2559_*2560insTT
ENST00000371953.8:c.*2559_*2560insTT MANE Select	ENSP00000361021.3:n.*2559_*2560insTT
ENST00000371953.7:c.*2559_*2560insTT	ENSP00000361021.3:n.*2559_*2560insTT
NM_000314.5:c.*2559_*2560insTT	NP_000305.3:n.*2559_*2560insTT
NM_000314.6:c.*2559_*2560insTT	NP_000305.3:n.*2559_*2560insTT
NM_001304717.2:c.*2559_*2560insTT	NP_001291646.2:n.*2559_*2560insTT
NM_001304718.1:c.*2559_*2560insTT	NP_001291647.1:n.*2559_*2560insTT
XM_006717926.2:c.*2559_*2560insTT	XP_006717989.1:n.*2559_*2560insTT
XM_011539982.1:c.*2559_*2560insTT	XP_011538284.1:n.*2559_*2560insTT
XR_945791.1:n.4341_4342insTT
NM_000314.7:c.*2559_*2560insTT	NP_000305.3:n.*2559_*2560insTT
NM_001304717.5:c.*2559_*2560insTT	NP_001291646.4:n.*2559_*2560insTT
NM_001304718.2:c.*2559_*2560insTT	NP_001291647.1:n.*2559_*2560insTT
NM_000314.8:c.*2559_*2560insTT MANE Select	NP_000305.3:n.*2559_*2560insTT