Canonical Allele Identifier: CA409671969
Gene: RTEL1 HGNC NCBI
RTEL1-TNFRSF6B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63672576T>G , CM000682.2:g.63672576T>G GRCh38
NC_000020.10:g.62303929T>G , CM000682.1:g.62303929T>G GRCh37
NC_000020.9:g.61774373T>G NCBI36
NG_033901.1:g.19767T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000425905.7:n.394T>G (RTEL1)
ENST00000425905.6:c.394T>G (RTEL1)
ENST00000508582.7:c.792T>G (RTEL1) ENSP00000424307.2:p.Ile264Met
ENST00000684971.1:n.1151T>G (RTEL1)
ENST00000686756.1:n.1038T>G (RTEL1)
ENST00000687123.1:n.550T>G (RTEL1)
ENST00000692658.1:n.1158T>G (RTEL1)
ENST00000692911.1:n.1447T>G (RTEL1)
ENST00000318100.9:c.51T>G (RTEL1) ENSP00000322287.5:p.Ile17Met
ENST00000360203.11:c.720T>G (RTEL1) MANE Select ENSP00000353332.5:p.Ile240Met
ENST00000482936.6:c.720T>G (RTEL1) ENSP00000457868.2:p.Ile240Met
ENST00000318100.8:c.51T>G (RTEL1) ENSP00000322287.5:p.Ile17Met
ENST00000356810.5:c.870T>G (RTEL1) ENSP00000349265.4:p.Ile290Met
ENST00000360203.9:c.720T>G (RTEL1) ENSP00000353332.5:p.Ile240Met
ENST00000370018.7:c.720T>G (RTEL1) ENSP00000359035.3:p.Ile240Met
ENST00000463361.1:n.417T>G (RTEL1)
ENST00000482936.5:c.720T>G (RTEL1-TNFRSF6B) ENSP00000457868.1:p.Ile240Met
ENST00000492259.6:c.720T>G (RTEL1-TNFRSF6B) ENSP00000457428.1:p.Ile240Met
ENST00000508582.6:c.792T>G (RTEL1) ENSP00000424307.2:p.Ile264Met
NM_001283009.1:c.720T>G (RTEL1) NP_001269938.1:p.Ile240Met
NM_001283010.1:c.51T>G (RTEL1) NP_001269939.1:p.Ile17Met
NM_016434.3:c.720T>G (RTEL1) NP_057518.1:p.Ile240Met
NM_032957.4:c.792T>G (RTEL1) NP_116575.3:p.Ile264Met
NR_037882.1:n.1547T>G (RTEL1-TNFRSF6B)
NM_001283009.2:c.720T>G (RTEL1) MANE Select NP_001269938.1:p.Ile240Met
NM_016434.4:c.720T>G (RTEL1) NP_057518.1:p.Ile240Met
NM_032957.5:c.792T>G (RTEL1) NP_116575.3:p.Ile264Met