Canonical Allele Identifier: CA1740720417
Gene: POT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124842894T= , CM000669.2:g.124842894T= GRCh38
NC_000007.13:g.124482948T= , CM000669.1:g.124482948T= GRCh37
NC_000007.12:g.124270184T= NCBI36
NG_029232.1:g.92090A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357628.8:c.1076A= MANE Select ENSP00000350249.3:p.Gln359=
ENST00000430927.6:c.1076A= ENSP00000397632.2:p.Gln359=
ENST00000653241.1:c.1076A= ENSP00000499476.1:p.Gln359=
ENST00000653274.1:c.1076A= ENSP00000499382.1:p.Gln359=
ENST00000653819.1:c.*807A= ENSP00000499533.1:n.*807A=
ENST00000653892.1:c.*718A= ENSP00000499506.1:n.*718A=
ENST00000654766.1:c.1076A= ENSP00000499395.1:p.Gln359=
ENST00000655761.1:c.1076A= ENSP00000499635.1:p.Gln359=
ENST00000657333.1:c.*807A= ENSP00000499425.1:n.*807A=
ENST00000657892.1:c.*945A= ENSP00000499524.1:n.*945A=
ENST00000661898.1:c.1076A= ENSP00000499528.1:p.Gln359=
ENST00000662531.1:c.*971A= ENSP00000499488.1:n.*971A=
ENST00000664330.1:c.*927A= ENSP00000499781.1:n.*927A=
ENST00000664366.1:c.1076A= ENSP00000499290.1:p.Gln359=
ENST00000668382.1:c.1076A= ENSP00000499546.1:p.Gln359=
ENST00000357628.7:c.1076A= ENSP00000350249.3:p.Gln359=
ENST00000393329.5:c.683A= ENSP00000377002.1:p.Gln228=
ENST00000466483.1:n.356A=
ENST00000607932.5:c.1076A= ENSP00000476506.1:p.Gln359=
ENST00000608057.5:c.*173A= ENSP00000476371.1:n.*173A=
ENST00000609106.5:c.1076A= ENSP00000476981.1:p.Gln359=
NM_001042594.1:c.683A= NP_001036059.1:p.Gln228=
NM_015450.2:c.1076A= NP_056265.2:p.Gln359=
NR_003102.1:n.1797A=
NR_003103.1:n.1677A=
NR_003104.1:n.1677A=
XM_006715917.2:c.1076A= XP_006715980.1:p.Gln359=
XM_011516006.1:c.683A= XP_011514308.1:p.Gln228=
XM_011516007.1:c.683A= XP_011514309.1:p.Gln228=
XM_006715917.4:c.1076A= XP_006715980.1:p.Gln359=
XM_017011942.2:c.683A= XP_016867431.1:p.Gln228=
XR_001744618.1:n.1667A=
XR_001744619.2:n.1536A=
NM_015450.3:c.1076A= MANE Select NP_056265.2:p.Gln359=
NM_001042594.2:c.683A= NP_001036059.1:p.Gln228=
NR_003102.2:n.1639A=
NR_003103.2:n.1519A=
NR_003104.2:n.1519A=