Canonical Allele Identifier: CA9965959

Gene: RTEL1-TNFRSF6B RTEL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63694973C>A , CM000682.2:g.63694973C>A	GRCh38
NC_000020.10:g.62326326C>A , CM000682.1:g.62326326C>A	GRCh37
NC_000020.9:g.61796770C>A	NCBI36
NG_033901.1:g.42164C>A
NG_046961.1:g.3323C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001283009.2:c.3342C>A (RTEL1) MANE Select	NP_001269938.1:p.His1114Gln
ENST00000360203.11:c.3342C>A (RTEL1) MANE Select	ENSP00000353332.5:p.His1114Gln
NM_001283009.1:c.3342C>A (RTEL1)	NP_001269938.1:p.His1114Gln
NM_001283010.1:c.2673C>A (RTEL1)	NP_001269939.1:p.His891Gln
NM_016434.3:c.3342C>A (RTEL1)	NP_057518.1:p.His1114Gln
NM_016434.4:c.3342C>A (RTEL1)	NP_057518.1:p.His1114Gln
NM_032957.4:c.3414C>A (RTEL1)	NP_116575.3:p.His1138Gln
NM_032957.5:c.3414C>A (RTEL1)	NP_116575.3:p.His1138Gln
NR_037882.1:n.4169C>A (RTEL1-TNFRSF6B)
ENST00000318100.8:c.2673C>A (RTEL1)	ENSP00000322287.5:p.His891Gln
ENST00000318100.9:c.2673C>A (RTEL1)	ENSP00000322287.5:p.His891Gln
ENST00000360203.9:c.3342C>A (RTEL1)	ENSP00000353332.5:p.His1114Gln
ENST00000370003.2:c.1077C>A (RTEL1)	ENSP00000359020.1:p.His359Gln
ENST00000370018.7:c.3342C>A (RTEL1)	ENSP00000359035.3:p.His1114Gln
ENST00000480273.5:n.3427C>A (RTEL1-TNFRSF6B)
ENST00000482936.5:c.3342C>A (RTEL1-TNFRSF6B)	ENSP00000457868.1:p.His1114Gln
ENST00000492259.6:c.*944C>A (RTEL1-TNFRSF6B)	ENSP00000457428.1:n.*944C>A
ENST00000496281.1:n.2824C>A (RTEL1-TNFRSF6B)
ENST00000496281.2:n.3353C>A (RTEL1-TNFRSF6B)
ENST00000496816.5:c.1274C>A (RTEL1)	ENSP00000425576.1:n.1274C>A
ENST00000508582.6:c.3414C>A (RTEL1)	ENSP00000424307.2:p.His1138Gln
ENST00000508582.7:c.3414C>A (RTEL1)	ENSP00000424307.2:p.His1138Gln
ENST00000697815.1:n.2089C>A (RTEL1-TNFRSF6B)