Canonical Allele Identifier: CA1926142772

Gene: PTEN KLLN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863189_87863192delinsCCCA , CM000672.2:g.87863189_87863192delinsCCCA	GRCh38
NC_000010.10:g.89622946_89622949delinsCCCA , CM000672.1:g.89622946_89622949delinsCCCA	GRCh37
NC_000010.9:g.89612926_89612929delinsCCCA	NCBI36
NG_007466.2:g.4752_4755delinsCCCA , LRG_311:g.4752_4755delinsCCCA
NG_033079.1:g.5246_5249delinsTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706954.1:c.-17+547_-17+550delinsCCCA (PTEN)	ENSP00000516674.1:n.-17+547_-17+550delinsCCCA
ENST00000688308.1:c.-17+76_-17+79delinsCCCA (PTEN)	ENSP00000508752.1:n.-17+76_-17+79delinsCCCA
ENST00000445946.5:c.-705_-702delinsTGGG (KLLN) MANE Select	ENSP00000392204.2:n.-705_-702delinsTGGG
ENST00000371953.7:c.-1281_-1278delinsCCCA (PTEN)	ENSP00000361021.3:n.-1281_-1278delinsCCCA
ENST00000445946.3:c.-705_-702delinsTGGG (KLLN)	ENSP00000392204.2:n.-705_-702delinsTGGG
NM_001126049.1:c.-705_-702delinsTGGG (KLLN)	NP_001119521.1:n.-705_-702delinsTGGG
NM_001126049.2:c.-705_-702delinsTGGG (KLLN) MANE Select	NP_001119521.1:n.-705_-702delinsTGGG