Canonical Allele Identifier: CA2610046162

Gene: PTEN KLLN

Linked Data

• gnomAD v4: 10-87863440-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863440T>C , CM000672.2:g.87863440T>C	GRCh38
NC_000010.10:g.89623197T>C , CM000672.1:g.89623197T>C	GRCh37
NC_000010.9:g.89613177T>C	NCBI36
NG_007466.2:g.5003T>C , LRG_311:g.5003T>C
NG_033079.1:g.4998A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706954.1:c.-17+798T>C (PTEN)	ENSP00000516674.1:n.-17+798T>C
ENST00000688308.1:c.-17+327T>C (PTEN)	ENSP00000508752.1:n.-17+327T>C
ENST00000693560.1:c.-510T>C (PTEN)	ENSP00000509861.1:n.-510T>C
ENST00000445946.5:c.-953A>G (KLLN) MANE Select	ENSP00000392204.2:n.-953A>G
ENST00000371953.7:c.-1030T>C (PTEN)	ENSP00000361021.3:n.-1030T>C
ENST00000610634.1:c.-1132T>C (PTEN)	ENSP00000477517.1:n.-1132T>C
NM_000314.5:c.-1029T>C (PTEN)	NP_000305.3:n.-1029T>C
NM_000314.6:c.-1029T>C (PTEN)	NP_000305.3:n.-1029T>C
NM_001304717.2:c.-510T>C (PTEN)	NP_001291646.2:n.-510T>C
NM_001304718.1:c.-1734T>C (PTEN)	NP_001291647.1:n.-1734T>C
NM_001126049.2:c.-953A>G (KLLN) MANE Select	NP_001119521.1:n.-953A>G