Canonical Allele Identifier: CA4465244
Gene: POT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124842947C>T , CM000669.2:g.124842947C>T GRCh38
NC_000007.13:g.124483001C>T , CM000669.1:g.124483001C>T GRCh37
NC_000007.12:g.124270237C>T NCBI36
NG_029232.1:g.92037G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357628.8:c.1023G>A MANE Select ENSP00000350249.3:p.Gln341=
ENST00000430927.6:c.1023G>A ENSP00000397632.2:p.Gln341=
ENST00000446993.6:c.630G>A ENSP00000388921.2:p.Gln210=
ENST00000653241.1:c.1023G>A ENSP00000499476.1:p.Gln341=
ENST00000653274.1:c.1023G>A ENSP00000499382.1:p.Gln341=
ENST00000653819.1:c.*754G>A ENSP00000499533.1:n.*754G>A
ENST00000653892.1:c.*665G>A ENSP00000499506.1:n.*665G>A
ENST00000654766.1:c.1023G>A ENSP00000499395.1:p.Gln341=
ENST00000655761.1:c.1023G>A ENSP00000499635.1:p.Gln341=
ENST00000657333.1:c.*754G>A ENSP00000499425.1:n.*754G>A
ENST00000657892.1:c.*892G>A ENSP00000499524.1:n.*892G>A
ENST00000661898.1:c.1023G>A ENSP00000499528.1:p.Gln341=
ENST00000662531.1:c.*918G>A ENSP00000499488.1:n.*918G>A
ENST00000664330.1:c.*874G>A ENSP00000499781.1:n.*874G>A
ENST00000664366.1:c.1023G>A ENSP00000499290.1:p.Gln341=
ENST00000668382.1:c.1023G>A ENSP00000499546.1:p.Gln341=
ENST00000357628.7:c.1023G>A ENSP00000350249.3:p.Gln341=
ENST00000393329.5:c.630G>A ENSP00000377002.1:p.Gln210=
ENST00000466483.1:n.303G>A
ENST00000607932.5:c.1023G>A ENSP00000476506.1:p.Gln341=
ENST00000608057.5:c.*120G>A ENSP00000476371.1:n.*120G>A
ENST00000609106.5:c.1023G>A ENSP00000476981.1:p.Gln341=
NM_001042594.1:c.630G>A NP_001036059.1:p.Gln210=
NM_015450.2:c.1023G>A NP_056265.2:p.Gln341=
NR_003102.1:n.1744G>A
NR_003103.1:n.1624G>A
NR_003104.1:n.1624G>A
XM_006715917.2:c.1023G>A XP_006715980.1:p.Gln341=
XM_011516006.1:c.630G>A XP_011514308.1:p.Gln210=
XM_011516007.1:c.630G>A XP_011514309.1:p.Gln210=
XM_006715917.4:c.1023G>A XP_006715980.1:p.Gln341=
XM_017011942.2:c.630G>A XP_016867431.1:p.Gln210=
XR_001744618.1:n.1614G>A
XR_001744619.2:n.1483G>A
NM_015450.3:c.1023G>A MANE Select NP_056265.2:p.Gln341=
NM_001042594.2:c.630G>A NP_001036059.1:p.Gln210=
NR_003102.2:n.1586G>A
NR_003103.2:n.1466G>A
NR_003104.2:n.1466G>A