Canonical Allele Identifier: CA14782096
Gene: RTEL1 HGNC NCBI
RTEL1-TNFRSF6B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63661765C>T , CM000682.2:g.63661765C>T GRCh38
NC_000020.10:g.62293118C>T , CM000682.1:g.62293118C>T GRCh37
NC_000020.9:g.61763562C>T NCBI36
NG_033901.1:g.8956C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001283009.2:c.302-85C>T (RTEL1) MANE Select NP_001269938.1:n.302-85C>T
ENST00000360203.11:c.302-85C>T (RTEL1) MANE Select ENSP00000353332.5:n.302-85C>T
NM_001283009.1:c.302-85C>T (RTEL1) NP_001269938.1:n.302-85C>T
NM_001283010.1:c.-368-85C>T (RTEL1) NP_001269939.1:n.-368-85C>T
NM_016434.3:c.302-85C>T (RTEL1) NP_057518.1:n.302-85C>T
NM_016434.4:c.302-85C>T (RTEL1) NP_057518.1:n.302-85C>T
NM_032957.4:c.302-85C>T (RTEL1) NP_116575.3:n.302-85C>T
NM_032957.5:c.302-85C>T (RTEL1) NP_116575.3:n.302-85C>T
NR_037882.1:n.1129-85C>T (RTEL1-TNFRSF6B)
ENST00000318100.8:c.-368-85C>T (RTEL1) ENSP00000322287.5:n.-368-85C>T
ENST00000318100.9:c.-368-85C>T (RTEL1) ENSP00000322287.5:n.-368-85C>T
ENST00000356810.5:c.302-85C>T (RTEL1) ENSP00000349265.4:n.302-85C>T
ENST00000360203.9:c.302-85C>T (RTEL1) ENSP00000353332.5:n.302-85C>T
ENST00000370018.7:c.302-85C>T (RTEL1) ENSP00000359035.3:n.302-85C>T
ENST00000482936.5:c.302-85C>T (RTEL1-TNFRSF6B) ENSP00000457868.1:n.302-85C>T
ENST00000482936.6:c.302-85C>T (RTEL1) ENSP00000457868.2:n.302-85C>T
ENST00000488316.1:n.577C>T (RTEL1)
ENST00000488316.2:n.593C>T (RTEL1)
ENST00000492259.6:c.302-85C>T (RTEL1-TNFRSF6B) ENSP00000457428.1:n.302-85C>T
ENST00000508582.6:c.302-85C>T (RTEL1) ENSP00000424307.2:n.302-85C>T
ENST00000508582.7:c.302-85C>T (RTEL1) ENSP00000424307.2:n.302-85C>T
ENST00000684971.1:n.648C>T (RTEL1)
ENST00000686756.1:n.620-85C>T (RTEL1)
ENST00000687123.1:n.47C>T (RTEL1)
ENST00000692658.1:n.655C>T (RTEL1)
ENST00000692911.1:n.1029-85C>T (RTEL1)