Canonical Allele Identifier: CA2374930813

Gene: RTEL1 RTEL1-TNFRSF6B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63689821C= , CM000682.2:g.63689821C=	GRCh38
NC_000020.10:g.62321174C= , CM000682.1:g.62321174C=	GRCh37
NC_000020.9:g.61791618C=	NCBI36
NG_033901.1:g.37012C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001283009.2:c.2097C= (RTEL1) MANE Select	NP_001269938.1:p.Ile699=
ENST00000360203.11:c.2097C= (RTEL1) MANE Select	ENSP00000353332.5:p.Ile699=
NM_001283009.1:c.2097C= (RTEL1)	NP_001269938.1:p.Ile699=
NM_001283010.1:c.1428C= (RTEL1)	NP_001269939.1:p.Ile476=
NM_016434.3:c.2097C= (RTEL1)	NP_057518.1:p.Ile699=
NM_016434.4:c.2097C= (RTEL1)	NP_057518.1:p.Ile699=
NM_032957.4:c.2169C= (RTEL1)	NP_116575.3:p.Ile723=
NM_032957.5:c.2169C= (RTEL1)	NP_116575.3:p.Ile723=
NR_037882.1:n.2924C= (RTEL1-TNFRSF6B)
ENST00000318100.8:c.1428C= (RTEL1)	ENSP00000322287.5:p.Ile476=
ENST00000318100.9:c.1428C= (RTEL1)	ENSP00000322287.5:p.Ile476=
ENST00000360203.9:c.2097C= (RTEL1)	ENSP00000353332.5:p.Ile699=
ENST00000370018.7:c.2097C= (RTEL1)	ENSP00000359035.3:p.Ile699=
ENST00000425905.5:c.276C= (RTEL1)	ENSP00000388063.1:p.Ile92=
ENST00000425905.6:c.1624C= (RTEL1)
ENST00000425905.7:n.1624C= (RTEL1)
ENST00000480273.5:n.2182C= (RTEL1-TNFRSF6B)
ENST00000482936.5:c.2097C= (RTEL1-TNFRSF6B)	ENSP00000457868.1:p.Ile699=
ENST00000482936.6:c.2097C= (RTEL1)	ENSP00000457868.2:p.Ile699=
ENST00000492259.6:c.2181C= (RTEL1-TNFRSF6B)	ENSP00000457428.1:p.Ile727=
ENST00000496281.1:n.391C= (RTEL1-TNFRSF6B)
ENST00000496281.2:n.920C= (RTEL1-TNFRSF6B)
ENST00000508582.6:c.2169C= (RTEL1)	ENSP00000424307.2:p.Ile723=
ENST00000508582.7:c.2169C= (RTEL1)	ENSP00000424307.2:p.Ile723=
ENST00000687123.1:n.1780C= (RTEL1)
ENST00000697814.1:n.287C= (RTEL1)
ENST00000697815.1:n.56C= (RTEL1-TNFRSF6B)