Canonical Allele Identifier: CA9964727

Gene: RTEL1 RTEL1-TNFRSF6B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63685825C>T , CM000682.2:g.63685825C>T	GRCh38
NC_000020.10:g.62317178C>T , CM000682.1:g.62317178C>T	GRCh37
NC_000020.9:g.61787622C>T	NCBI36
NG_033901.1:g.33016C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001283009.2:c.1301C>T (RTEL1) MANE Select	NP_001269938.1:p.Thr434Met
ENST00000360203.11:c.1301C>T (RTEL1) MANE Select	ENSP00000353332.5:p.Thr434Met
NM_001283009.1:c.1301C>T (RTEL1)	NP_001269938.1:p.Thr434Met
NM_001283010.1:c.632C>T (RTEL1)	NP_001269939.1:p.Thr211Met
NM_016434.3:c.1301C>T (RTEL1)	NP_057518.1:p.Thr434Met
NM_016434.4:c.1301C>T (RTEL1)	NP_057518.1:p.Thr434Met
NM_032957.4:c.1373C>T (RTEL1)	NP_116575.3:p.Thr458Met
NM_032957.5:c.1373C>T (RTEL1)	NP_116575.3:p.Thr458Met
NR_037882.1:n.2128C>T (RTEL1-TNFRSF6B)
ENST00000318100.8:c.632C>T (RTEL1)	ENSP00000322287.5:p.Thr211Met
ENST00000318100.9:c.632C>T (RTEL1)	ENSP00000322287.5:p.Thr211Met
ENST00000360203.9:c.1301C>T (RTEL1)	ENSP00000353332.5:p.Thr434Met
ENST00000370018.7:c.1301C>T (RTEL1)	ENSP00000359035.3:p.Thr434Met
ENST00000425905.6:c.975C>T (RTEL1)
ENST00000425905.7:n.975C>T (RTEL1)
ENST00000482936.5:c.1301C>T (RTEL1-TNFRSF6B)	ENSP00000457868.1:p.Thr434Met
ENST00000482936.6:c.1301C>T (RTEL1)	ENSP00000457868.2:p.Thr434Met
ENST00000492259.6:c.1385C>T (RTEL1-TNFRSF6B)	ENSP00000457428.1:p.Thr462Met
ENST00000508582.6:c.1373C>T (RTEL1)	ENSP00000424307.2:p.Thr458Met
ENST00000508582.7:c.1373C>T (RTEL1)	ENSP00000424307.2:p.Thr458Met
ENST00000647249.1:n.232C>T (RTEL1)
ENST00000687123.1:n.1131C>T (RTEL1)