Canonical Allele Identifier: CA2610046166

Gene: PTEN KLLN

Linked Data

• gnomAD v4: 10-87863441-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863441C>A , CM000672.2:g.87863441C>A	GRCh38
NC_000010.10:g.89623198C>A , CM000672.1:g.89623198C>A	GRCh37
NC_000010.9:g.89613178C>A	NCBI36
NG_007466.2:g.5004C>A , LRG_311:g.5004C>A
NG_033079.1:g.4997G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000706954.1:c.-17+799C>A (PTEN)	ENSP00000516674.1:n.-17+799C>A
ENST00000688308.1:c.-17+328C>A (PTEN)	ENSP00000508752.1:n.-17+328C>A
ENST00000693560.1:c.-509C>A (PTEN)	ENSP00000509861.1:n.-509C>A
ENST00000445946.5:c.-954G>T (KLLN) MANE Select	ENSP00000392204.2:n.-954G>T
ENST00000371953.7:c.-1029C>A (PTEN)	ENSP00000361021.3:n.-1029C>A
ENST00000610634.1:c.-1131C>A (PTEN)	ENSP00000477517.1:n.-1131C>A
NM_000314.5:c.-1028C>A (PTEN)	NP_000305.3:n.-1028C>A
NM_000314.6:c.-1028C>A (PTEN)	NP_000305.3:n.-1028C>A
NM_001304717.2:c.-509C>A (PTEN)	NP_001291646.2:n.-509C>A
NM_001304718.1:c.-1733C>A (PTEN)	NP_001291647.1:n.-1733C>A
NM_001126049.2:c.-954G>T (KLLN) MANE Select	NP_001119521.1:n.-954G>T