Canonical Allele Identifier: CA1926142847

Gene: PTEN KLLN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863290_87863291delinsAG , CM000672.2:g.87863290_87863291delinsAG	GRCh38
NC_000010.10:g.89623047_89623048delinsAG , CM000672.1:g.89623047_89623048delinsAG	GRCh37
NC_000010.9:g.89613027_89613028delinsAG	NCBI36
NG_007466.2:g.4853_4854delinsAG , LRG_311:g.4853_4854delinsAG
NG_033079.1:g.5147_5148delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706954.1:c.-17+648_-17+649delinsAG (PTEN)	ENSP00000516674.1:n.-17+648_-17+649delinsAG
ENST00000688308.1:c.-17+177_-17+178delinsAG (PTEN)	ENSP00000508752.1:n.-17+177_-17+178delinsAG
ENST00000445946.5:c.-804_-803delinsCT (KLLN) MANE Select	ENSP00000392204.2:n.-804_-803delinsCT
ENST00000371953.7:c.-1180_-1179delinsAG (PTEN)	ENSP00000361021.3:n.-1180_-1179delinsAG
ENST00000445946.3:c.-804_-803delinsCT (KLLN)	ENSP00000392204.2:n.-804_-803delinsCT
NM_001126049.1:c.-804_-803delinsCT (KLLN)	NP_001119521.1:n.-804_-803delinsCT
NM_001126049.2:c.-804_-803delinsCT (KLLN) MANE Select	NP_001119521.1:n.-804_-803delinsCT