Canonical Allele Identifier: CA377786285

Gene: PTEN KLLN

Linked Data

• ClinVar Variation Id: 1750483
• ClinVar RCV Id: RCV002355787
• MyVariant Identifiers: chr10:g.87863258C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863258C>T , CM000672.2:g.87863258C>T	GRCh38
NC_000010.10:g.89623015C>T , CM000672.1:g.89623015C>T	GRCh37
NC_000010.9:g.89612995C>T	NCBI36
NG_007466.2:g.4821C>T , LRG_311:g.4821C>T
NG_033079.1:g.5180G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706954.1:c.-17+616C>T (PTEN)	ENSP00000516674.1:n.-17+616C>T
ENST00000688308.1:c.-17+145C>T (PTEN)	ENSP00000508752.1:n.-17+145C>T
ENST00000445946.5:c.-771G>A (KLLN) MANE Select	ENSP00000392204.2:n.-771G>A
ENST00000371953.7:c.-1212C>T (PTEN)	ENSP00000361021.3:n.-1212C>T
ENST00000445946.3:c.-771G>A (KLLN)	ENSP00000392204.2:n.-771G>A
NM_001126049.1:c.-771G>A (KLLN)	NP_001119521.1:n.-771G>A
NM_001126049.2:c.-771G>A (KLLN) MANE Select	NP_001119521.1:n.-771G>A