Canonical Allele Identifier: CA14782128
Gene: RTEL1 HGNC NCBI
RTEL1-TNFRSF6B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63685277C>T , CM000682.2:g.63685277C>T GRCh38
NC_000020.10:g.62316630C>T , CM000682.1:g.62316630C>T GRCh37
NC_000020.9:g.61787074C>T NCBI36
NG_033901.1:g.32468C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000425905.7:n.866-246C>T (RTEL1)
ENST00000425905.6:c.866-246C>T (RTEL1)
ENST00000508582.7:c.1264-246C>T (RTEL1) ENSP00000424307.2:n.1264-246C>T
ENST00000687123.1:n.1022-246C>T (RTEL1)
ENST00000318100.9:c.523-246C>T (RTEL1) ENSP00000322287.5:n.523-246C>T
ENST00000360203.11:c.1192-246C>T (RTEL1) MANE Select ENSP00000353332.5:n.1192-246C>T
ENST00000482936.6:c.1192-246C>T (RTEL1) ENSP00000457868.2:n.1192-246C>T
ENST00000647249.1:n.123-246C>T (RTEL1)
ENST00000318100.8:c.523-246C>T (RTEL1) ENSP00000322287.5:n.523-246C>T
ENST00000360203.9:c.1192-246C>T (RTEL1) ENSP00000353332.5:n.1192-246C>T
ENST00000370018.7:c.1192-246C>T (RTEL1) ENSP00000359035.3:n.1192-246C>T
ENST00000482936.5:c.1192-246C>T (RTEL1-TNFRSF6B) ENSP00000457868.1:n.1192-246C>T
ENST00000492259.6:c.1276-246C>T (RTEL1-TNFRSF6B) ENSP00000457428.1:n.1276-246C>T
ENST00000508582.6:c.1264-246C>T (RTEL1) ENSP00000424307.2:n.1264-246C>T
NM_001283009.1:c.1192-246C>T (RTEL1) NP_001269938.1:n.1192-246C>T
NM_001283010.1:c.523-246C>T (RTEL1) NP_001269939.1:n.523-246C>T
NM_016434.3:c.1192-246C>T (RTEL1) NP_057518.1:n.1192-246C>T
NM_032957.4:c.1264-246C>T (RTEL1) NP_116575.3:n.1264-246C>T
NR_037882.1:n.2019-246C>T (RTEL1-TNFRSF6B)
NM_001283009.2:c.1192-246C>T (RTEL1) MANE Select NP_001269938.1:n.1192-246C>T
NM_016434.4:c.1192-246C>T (RTEL1) NP_057518.1:n.1192-246C>T
NM_032957.5:c.1264-246C>T (RTEL1) NP_116575.3:n.1264-246C>T