Canonical Allele Identifier: CA2610046342

Gene: PTEN KLLN

Linked Data

• gnomAD v4: 10-87863518-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863518C>G , CM000672.2:g.87863518C>G	GRCh38
NC_000010.10:g.89623275C>G , CM000672.1:g.89623275C>G	GRCh37
NC_000010.9:g.89613255C>G	NCBI36
NG_007466.2:g.5081C>G , LRG_311:g.5081C>G
NG_033079.1:g.4920G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706954.1:c.-17+876C>G (PTEN)	ENSP00000516674.1:n.-17+876C>G
ENST00000688308.1:c.-17+405C>G (PTEN)	ENSP00000508752.1:n.-17+405C>G
ENST00000693560.1:c.-432C>G (PTEN)	ENSP00000509861.1:n.-432C>G
ENST00000445946.5:c.-1031G>C (KLLN) MANE Select	ENSP00000392204.2:n.-1031G>C
ENST00000371953.7:c.-952C>G (PTEN)	ENSP00000361021.3:n.-952C>G
ENST00000610634.1:c.-1054C>G (PTEN)	ENSP00000477517.1:n.-1054C>G
NM_000314.5:c.-951C>G (PTEN)	NP_000305.3:n.-951C>G
NM_000314.6:c.-951C>G (PTEN)	NP_000305.3:n.-951C>G
NM_001304717.2:c.-432C>G (PTEN)	NP_001291646.2:n.-432C>G
NM_001304718.1:c.-1656C>G (PTEN)	NP_001291647.1:n.-1656C>G
NM_001126049.2:c.-1031G>C (KLLN) MANE Select	NP_001119521.1:n.-1031G>C