Canonical Allele Identifier: CA369053741

Gene: POT1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.124846962C>T , CM000669.2:g.124846962C>T	GRCh38
NC_000007.13:g.124487016C>T , CM000669.1:g.124487016C>T	GRCh37
NC_000007.12:g.124274252C>T	NCBI36
NG_029232.1:g.88022G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015450.3:c.986G>A MANE Select	NP_056265.2:p.Cys329Tyr
ENST00000357628.8:c.986G>A MANE Select	ENSP00000350249.3:p.Cys329Tyr
NM_001042594.1:c.593G>A	NP_001036059.1:p.Cys198Tyr
NM_001042594.2:c.593G>A	NP_001036059.1:p.Cys198Tyr
NM_015450.2:c.986G>A	NP_056265.2:p.Cys329Tyr
NR_003102.1:n.1707G>A
NR_003102.2:n.1549G>A
NR_003103.1:n.1587G>A
NR_003103.2:n.1429G>A
NR_003104.1:n.1587G>A
NR_003104.2:n.1429G>A
ENST00000357628.7:c.986G>A	ENSP00000350249.3:p.Cys329Tyr
ENST00000393329.5:c.593G>A	ENSP00000377002.1:p.Cys198Tyr
ENST00000430927.6:c.986G>A	ENSP00000397632.2:p.Cys329Tyr
ENST00000446993.6:c.593G>A	ENSP00000388921.2:p.Cys198Tyr
ENST00000607932.5:c.986G>A	ENSP00000476506.1:p.Cys329Tyr
ENST00000608057.5:c.*83G>A	ENSP00000476371.1:n.*83G>A
ENST00000609106.5:c.986G>A	ENSP00000476981.1:p.Cys329Tyr
ENST00000653241.1:c.986G>A	ENSP00000499476.1:p.Cys329Tyr
ENST00000653274.1:c.986G>A	ENSP00000499382.1:p.Cys329Tyr
ENST00000653819.1:c.*717G>A	ENSP00000499533.1:n.*717G>A
ENST00000653892.1:c.*628G>A	ENSP00000499506.1:n.*628G>A
ENST00000654766.1:c.986G>A	ENSP00000499395.1:p.Cys329Tyr
ENST00000655761.1:c.986G>A	ENSP00000499635.1:p.Cys329Tyr
ENST00000657333.1:c.*717G>A	ENSP00000499425.1:n.*717G>A
ENST00000657892.1:c.*855G>A	ENSP00000499524.1:n.*855G>A
ENST00000661898.1:c.986G>A	ENSP00000499528.1:p.Cys329Tyr
ENST00000662531.1:c.*881G>A	ENSP00000499488.1:n.*881G>A
ENST00000664330.1:c.*837G>A	ENSP00000499781.1:n.*837G>A
ENST00000664366.1:c.986G>A	ENSP00000499290.1:p.Cys329Tyr
ENST00000668382.1:c.986G>A	ENSP00000499546.1:p.Cys329Tyr
XM_006715917.2:c.986G>A	XP_006715980.1:p.Cys329Tyr
XM_006715917.4:c.986G>A	XP_006715980.1:p.Cys329Tyr
XM_011516006.1:c.593G>A	XP_011514308.1:p.Cys198Tyr
XM_011516007.1:c.593G>A	XP_011514309.1:p.Cys198Tyr
XM_017011942.2:c.593G>A	XP_016867431.1:p.Cys198Tyr
XR_001744618.1:n.1577G>A
XR_001744619.2:n.1446G>A