Canonical Allele Identifier: CA369068470

Gene: POT1

Linked Data

• MyVariant Identifiers: chr7:g.124482962T>A (hg19) ; chr7:g.124842908T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.124842908T>A , CM000669.2:g.124842908T>A	GRCh38
NC_000007.13:g.124482962T>A , CM000669.1:g.124482962T>A	GRCh37
NC_000007.12:g.124270198T>A	NCBI36
NG_029232.1:g.92076A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357628.8:c.1062A>T MANE Select	ENSP00000350249.3:p.Gln354His
ENST00000430927.6:c.1062A>T	ENSP00000397632.2:p.Gln354His
ENST00000653241.1:c.1062A>T	ENSP00000499476.1:p.Gln354His
ENST00000653274.1:c.1062A>T	ENSP00000499382.1:p.Gln354His
ENST00000653819.1:c.*793A>T	ENSP00000499533.1:n.*793A>T
ENST00000653892.1:c.*704A>T	ENSP00000499506.1:n.*704A>T
ENST00000654766.1:c.1062A>T	ENSP00000499395.1:p.Gln354His
ENST00000655761.1:c.1062A>T	ENSP00000499635.1:p.Gln354His
ENST00000657333.1:c.*793A>T	ENSP00000499425.1:n.*793A>T
ENST00000657892.1:c.*931A>T	ENSP00000499524.1:n.*931A>T
ENST00000661898.1:c.1062A>T	ENSP00000499528.1:p.Gln354His
ENST00000662531.1:c.*957A>T	ENSP00000499488.1:n.*957A>T
ENST00000664330.1:c.*913A>T	ENSP00000499781.1:n.*913A>T
ENST00000664366.1:c.1062A>T	ENSP00000499290.1:p.Gln354His
ENST00000668382.1:c.1062A>T	ENSP00000499546.1:p.Gln354His
ENST00000357628.7:c.1062A>T	ENSP00000350249.3:p.Gln354His
ENST00000393329.5:c.669A>T	ENSP00000377002.1:p.Gln223His
ENST00000466483.1:n.342A>T
ENST00000607932.5:c.1062A>T	ENSP00000476506.1:p.Gln354His
ENST00000608057.5:c.*159A>T	ENSP00000476371.1:n.*159A>T
ENST00000609106.5:c.1062A>T	ENSP00000476981.1:p.Gln354His
NM_001042594.1:c.669A>T	NP_001036059.1:p.Gln223His
NM_015450.2:c.1062A>T	NP_056265.2:p.Gln354His
NR_003102.1:n.1783A>T
NR_003103.1:n.1663A>T
NR_003104.1:n.1663A>T
XM_006715917.2:c.1062A>T	XP_006715980.1:p.Gln354His
XM_011516006.1:c.669A>T	XP_011514308.1:p.Gln223His
XM_011516007.1:c.669A>T	XP_011514309.1:p.Gln223His
XM_006715917.4:c.1062A>T	XP_006715980.1:p.Gln354His
XM_017011942.2:c.669A>T	XP_016867431.1:p.Gln223His
XR_001744618.1:n.1653A>T
XR_001744619.2:n.1522A>T
NM_015450.3:c.1062A>T MANE Select	NP_056265.2:p.Gln354His
NM_001042594.2:c.669A>T	NP_001036059.1:p.Gln223His
NR_003102.2:n.1625A>T
NR_003103.2:n.1505A>T
NR_003104.2:n.1505A>T