Canonical Allele Identifier: CA369061676

Gene: POT1

Linked Data

• ClinVar Variation Id: 650374
• ClinVar RCV Id: RCV003322827
• dbSNP Id: rs1345686360
• gnomAD v2: 7-124511075-T-C
• gnomAD v3: 7-124871021-T-C
• gnomAD v4: 7-124871021-T-C
• MyVariant Identifiers: chr7:g.124511075T>C (hg19) ; chr7:g.124871021T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.124871021T>C , CM000669.2:g.124871021T>C	GRCh38
NC_000007.13:g.124511075T>C , CM000669.1:g.124511075T>C	GRCh37
NC_000007.12:g.124298311T>C	NCBI36
NG_029232.1:g.63963A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000357628.8:c.145A>G MANE Select	ENSP00000350249.3:p.Ile49Val
ENST00000429326.6:c.125-7381A>G	ENSP00000403088.1:n.125-7381A>G
ENST00000430927.6:c.145A>G	ENSP00000397632.2:p.Ile49Val
ENST00000446993.6:c.-249A>G	ENSP00000388921.2:n.-249A>G
ENST00000653241.1:c.145A>G	ENSP00000499476.1:p.Ile49Val
ENST00000653274.1:c.145A>G	ENSP00000499382.1:p.Ile49Val
ENST00000653819.1:c.125-7381A>G	ENSP00000499533.1:n.125-7381A>G
ENST00000653892.1:c.125-7381A>G	ENSP00000499506.1:n.125-7381A>G
ENST00000654766.1:c.145A>G	ENSP00000499395.1:p.Ile49Val
ENST00000655761.1:c.145A>G	ENSP00000499635.1:p.Ile49Val
ENST00000657333.1:c.125-7381A>G	ENSP00000499425.1:n.125-7381A>G
ENST00000657892.1:c.125-5722A>G	ENSP00000499524.1:n.125-5722A>G
ENST00000661898.1:c.145A>G	ENSP00000499528.1:p.Ile49Val
ENST00000662531.1:c.*40A>G	ENSP00000499488.1:n.*40A>G
ENST00000664330.1:c.125-7381A>G	ENSP00000499781.1:n.125-7381A>G
ENST00000664366.1:c.145A>G	ENSP00000499290.1:p.Ile49Val
ENST00000668382.1:c.145A>G	ENSP00000499546.1:p.Ile49Val
ENST00000357628.7:c.145A>G	ENSP00000350249.3:p.Ile49Val
ENST00000393329.5:c.-138-7381A>G	ENSP00000377002.1:n.-138-7381A>G
ENST00000429326.5:c.125-7381A>G	ENSP00000403088.1:n.125-7381A>G
ENST00000446993.5:c.145A>G	ENSP00000388921.1:p.Ile49Val
ENST00000607932.5:c.145A>G	ENSP00000476506.1:p.Ile49Val
ENST00000608057.5:c.145A>G	ENSP00000476371.1:p.Ile49Val
ENST00000609106.5:c.145A>G	ENSP00000476981.1:p.Ile49Val
ENST00000609702.5:c.145A>G	ENSP00000477258.1:p.Ile49Val
NM_001042594.1:c.-138-7381A>G	NP_001036059.1:n.-138-7381A>G
NM_015450.2:c.145A>G	NP_056265.2:p.Ile49Val
NR_003102.1:n.746A>G
NR_003103.1:n.746A>G
NR_003104.1:n.746A>G
XM_006715917.2:c.145A>G	XP_006715980.1:p.Ile49Val
XM_011516006.1:c.-249A>G	XP_011514308.1:n.-249A>G
XM_011516007.1:c.-249A>G	XP_011514309.1:n.-249A>G
XM_006715917.4:c.145A>G	XP_006715980.1:p.Ile49Val
XM_017011942.2:c.-138-7381A>G	XP_016867431.1:n.-138-7381A>G
XR_001744618.1:n.736A>G
XR_001744619.2:n.716-7381A>G
NM_015450.3:c.145A>G MANE Select	NP_056265.2:p.Ile49Val
NM_001042594.2:c.-138-7381A>G	NP_001036059.1:n.-138-7381A>G
NR_003102.2:n.588A>G
NR_003103.2:n.588A>G
NR_003104.2:n.588A>G