Canonical Allele Identifier: CA1926177076

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87967641G= , CM000672.2:g.87967641G=	GRCh38
NC_000010.10:g.89727398G= , CM000672.1:g.89727398G=	GRCh37
NC_000010.9:g.89717378G=	NCBI36
NG_007466.2:g.109203G= , LRG_311:g.109203G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*2410G=	ENSP00000518161.1:n.*2410G=
ENST00000688158.2:n.4116G=
ENST00000706954.1:c.*2169G=	ENSP00000516674.1:n.*2169G=
ENST00000706955.1:c.*3416G=	ENSP00000516675.1:n.*3416G=
ENST00000688158.1:c.*3492G=	ENSP00000509254.1:n.*3492G=
ENST00000693560.1:c.*2169G=	ENSP00000509861.1:n.*2169G=
ENST00000371953.8:c.*2169G= MANE Select	ENSP00000361021.3:n.*2169G=
ENST00000371953.7:c.*2169G=	ENSP00000361021.3:n.*2169G=
NM_000314.5:c.*2169G=	NP_000305.3:n.*2169G=
NM_000314.6:c.*2169G=	NP_000305.3:n.*2169G=
NM_001304717.2:c.*2169G=	NP_001291646.2:n.*2169G=
NM_001304718.1:c.*2169G=	NP_001291647.1:n.*2169G=
XM_006717926.2:c.*2169G=	XP_006717989.1:n.*2169G=
XM_011539982.1:c.*2169G=	XP_011538284.1:n.*2169G=
XR_945791.1:n.3951G=
NM_000314.7:c.*2169G=	NP_000305.3:n.*2169G=
NM_001304717.5:c.*2169G=	NP_001291646.4:n.*2169G=
NM_001304718.2:c.*2169G=	NP_001291647.1:n.*2169G=
NM_000314.8:c.*2169G= MANE Select	NP_000305.3:n.*2169G=