Canonical Allele Identifier: CA409672098
Gene: RTEL1 HGNC NCBI
RTEL1-TNFRSF6B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63672609A>C , CM000682.2:g.63672609A>C GRCh38
NC_000020.10:g.62303962A>C , CM000682.1:g.62303962A>C GRCh37
NC_000020.9:g.61774406A>C NCBI36
NG_033901.1:g.19800A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000425905.7:n.427A>C (RTEL1)
ENST00000425905.6:c.427A>C (RTEL1)
ENST00000508582.7:c.825A>C (RTEL1) ENSP00000424307.2:p.Glu275Asp
ENST00000684971.1:n.1184A>C (RTEL1)
ENST00000686756.1:n.1071A>C (RTEL1)
ENST00000687123.1:n.583A>C (RTEL1)
ENST00000692658.1:n.1191A>C (RTEL1)
ENST00000692911.1:n.1480A>C (RTEL1)
ENST00000318100.9:c.84A>C (RTEL1) ENSP00000322287.5:p.Glu28Asp
ENST00000360203.11:c.753A>C (RTEL1) MANE Select ENSP00000353332.5:p.Glu251Asp
ENST00000482936.6:c.753A>C (RTEL1) ENSP00000457868.2:p.Glu251Asp
ENST00000318100.8:c.84A>C (RTEL1) ENSP00000322287.5:p.Glu28Asp
ENST00000356810.5:c.903A>C (RTEL1) ENSP00000349265.4:p.Glu301Asp
ENST00000360203.9:c.753A>C (RTEL1) ENSP00000353332.5:p.Glu251Asp
ENST00000370018.7:c.753A>C (RTEL1) ENSP00000359035.3:p.Glu251Asp
ENST00000463361.1:n.450A>C (RTEL1)
ENST00000482936.5:c.753A>C (RTEL1-TNFRSF6B) ENSP00000457868.1:p.Glu251Asp
ENST00000492259.6:c.753A>C (RTEL1-TNFRSF6B) ENSP00000457428.1:p.Glu251Asp
ENST00000508582.6:c.825A>C (RTEL1) ENSP00000424307.2:p.Glu275Asp
NM_001283009.1:c.753A>C (RTEL1) NP_001269938.1:p.Glu251Asp
NM_001283010.1:c.84A>C (RTEL1) NP_001269939.1:p.Glu28Asp
NM_016434.3:c.753A>C (RTEL1) NP_057518.1:p.Glu251Asp
NM_032957.4:c.825A>C (RTEL1) NP_116575.3:p.Glu275Asp
NR_037882.1:n.1580A>C (RTEL1-TNFRSF6B)
NM_001283009.2:c.753A>C (RTEL1) MANE Select NP_001269938.1:p.Glu251Asp
NM_016434.4:c.753A>C (RTEL1) NP_057518.1:p.Glu251Asp
NM_032957.5:c.825A>C (RTEL1) NP_116575.3:p.Glu275Asp