Canonical Allele Identifier: CA1926143087

Gene: PTEN

Linked Data

• dbSNP Id: rs1858335021
• gnomAD v4: 10-87863545-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863545G>C , CM000672.2:g.87863545G>C	GRCh38
NC_000010.10:g.89623302G>C , CM000672.1:g.89623302G>C	GRCh37
NC_000010.9:g.89613282G>C	NCBI36
NG_007466.2:g.5108G>C , LRG_311:g.5108G>C
NG_033079.1:g.4893C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706954.1:c.-17+903G>C	ENSP00000516674.1:n.-17+903G>C
ENST00000688308.1:c.-17+432G>C	ENSP00000508752.1:n.-17+432G>C
ENST00000693560.1:c.-405G>C	ENSP00000509861.1:n.-405G>C
ENST00000371953.7:c.-925G>C	ENSP00000361021.3:n.-925G>C
ENST00000610634.1:c.-1027G>C	ENSP00000477517.1:n.-1027G>C
NM_000314.5:c.-924G>C	NP_000305.3:n.-924G>C
NM_000314.6:c.-924G>C	NP_000305.3:n.-924G>C
NM_001304717.2:c.-405G>C	NP_001291646.2:n.-405G>C
NM_001304718.1:c.-1629G>C	NP_001291647.1:n.-1629G>C