Canonical Allele Identifier: CA1926177206

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967730_87967733delinsCTGT , CM000672.2:g.87967730_87967733delinsCTGT	GRCh38
NC_000010.10:g.89727487_89727490delinsCTGT , CM000672.1:g.89727487_89727490delinsCTGT	GRCh37
NC_000010.9:g.89717467_89717470delinsCTGT	NCBI36
NG_007466.2:g.109292_109295delinsCTGT , LRG_311:g.109292_109295delinsCTGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*2499_*2502delinsCTGT	ENSP00000518161.1:n.*2499_*2502delinsCTGT...
ENST00000688158.2:n.4205_4208delinsCTGT
ENST00000706954.1:c.*2258_*2261delinsCTGT	ENSP00000516674.1:n.*2258_*2261delinsCTGT...
ENST00000706955.1:c.*3505_*3508delinsCTGT	ENSP00000516675.1:n.*3505_*3508delinsCTGT...
ENST00000688158.1:c.*3581_*3584delinsCTGT	ENSP00000509254.1:n.*3581_*3584delinsCTGT...
ENST00000693560.1:c.*2258_*2261delinsCTGT	ENSP00000509861.1:n.*2258_*2261delinsCTGT...
ENST00000371953.8:c.*2258_*2261delinsCTGT MANE Select	ENSP00000361021.3:n.*2258_*2261delinsCTGT...
ENST00000371953.7:c.*2258_*2261delinsCTGT	ENSP00000361021.3:n.*2258_*2261delinsCTGT...
NM_000314.5:c.*2258_*2261delinsCTGT	NP_000305.3:n.*2258_*2261delinsCTGT
NM_000314.6:c.*2258_*2261delinsCTGT	NP_000305.3:n.*2258_*2261delinsCTGT
NM_001304717.2:c.*2258_*2261delinsCTGT	NP_001291646.2:n.*2258_*2261delinsCTGT
NM_001304718.1:c.*2258_*2261delinsCTGT	NP_001291647.1:n.*2258_*2261delinsCTGT
XM_006717926.2:c.*2258_*2261delinsCTGT	XP_006717989.1:n.*2258_*2261delinsCTGT
XM_011539982.1:c.*2258_*2261delinsCTGT	XP_011538284.1:n.*2258_*2261delinsCTGT
XR_945791.1:n.4040_4043delinsCTGT
NM_000314.7:c.*2258_*2261delinsCTGT	NP_000305.3:n.*2258_*2261delinsCTGT
NM_001304717.5:c.*2258_*2261delinsCTGT	NP_001291646.4:n.*2258_*2261delinsCTGT
NM_001304718.2:c.*2258_*2261delinsCTGT	NP_001291647.1:n.*2258_*2261delinsCTGT
NM_000314.8:c.*2258_*2261delinsCTGT MANE Select	NP_000305.3:n.*2258_*2261delinsCTGT