Canonical Allele Identifier: CA211452709

Gene: PTEN MLDHR

Linked Data

• dbSNP Id: rs537241946
• MyVariant Identifiers: chr10:g.87863605C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863605C>G , CM000672.2:g.87863605C>G	GRCh38
NC_000010.10:g.89623362C>G , CM000672.1:g.89623362C>G	GRCh37
NC_000010.9:g.89613342C>G	NCBI36
NG_007466.2:g.5168C>G , LRG_311:g.5168C>G
NG_033079.1:g.4833G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706954.1:c.-16-849C>G (PTEN)	ENSP00000516674.1:n.-16-849C>G
ENST00000688308.1:c.-17+492C>G (PTEN)	ENSP00000508752.1:n.-17+492C>G
ENST00000692337.1:c.47C>G (MLDHR)	ENSP00000509326.1:p.Ala16Gly
ENST00000693560.1:c.-345C>G (PTEN)	ENSP00000509861.1:n.-345C>G
ENST00000371953.7:c.-865C>G (PTEN)	ENSP00000361021.3:n.-865C>G
ENST00000610634.1:c.-967C>G (PTEN)	ENSP00000477517.1:n.-967C>G
NM_000314.5:c.-864C>G (PTEN)	NP_000305.3:n.-864C>G
NM_000314.6:c.-864C>G (PTEN)	NP_000305.3:n.-864C>G
NM_001304717.2:c.-345C>G (PTEN)	NP_001291646.2:n.-345C>G
NM_001304718.1:c.-1569C>G (PTEN)	NP_001291647.1:n.-1569C>G