Canonical Allele Identifier: CA2374935909
Gene: RTEL1-TNFRSF6B HGNC NCBI
RTEL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63695704G= , CM000682.2:g.63695704G= GRCh38
NC_000020.10:g.62327057G= , CM000682.1:g.62327057G= GRCh37
NC_000020.9:g.61797501G= NCBI36
NG_033901.1:g.42895G=
NG_046961.1:g.4054G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697815.1:n.2569+54G= (RTEL1-TNFRSF6B)
ENST00000508582.7:c.3725-74G= (RTEL1) ENSP00000424307.2:n.3725-74G=
ENST00000318100.9:c.2984-74G= (RTEL1) ENSP00000322287.5:n.2984-74G=
ENST00000360203.11:c.3822+54G= (RTEL1) MANE Select ENSP00000353332.5:n.3822+54G=
ENST00000496281.2:n.3833+54G= (RTEL1-TNFRSF6B)
ENST00000318100.8:c.2984-74G= (RTEL1) ENSP00000322287.5:n.2984-74G=
ENST00000360203.9:c.3822+54G= (RTEL1) ENSP00000353332.5:n.3822+54G=
ENST00000370003.2:c.1557+54G= (RTEL1) ENSP00000359020.1:n.1557+54G=
ENST00000370018.7:c.3653-74G= (RTEL1) ENSP00000359035.3:n.3653-74G=
ENST00000480273.5:n.3738-74G= (RTEL1-TNFRSF6B)
ENST00000482936.5:c.3822+54G= (RTEL1-TNFRSF6B) ENSP00000457868.1:n.3822+54G=
ENST00000492259.6:c.*1255-74G= (RTEL1-TNFRSF6B) ENSP00000457428.1:n.*1255-74G=
ENST00000496281.1:n.3304+54G= (RTEL1-TNFRSF6B)
ENST00000496816.5:c.1754+54G= (RTEL1) ENSP00000425576.1:n.1754+54G=
ENST00000508582.6:c.3725-74G= (RTEL1) ENSP00000424307.2:n.3725-74G=
NM_001283009.1:c.3822+54G= (RTEL1) NP_001269938.1:n.3822+54G=
NM_001283010.1:c.2984-74G= (RTEL1) NP_001269939.1:n.2984-74G=
NM_016434.3:c.3653-74G= (RTEL1) NP_057518.1:n.3653-74G=
NM_032957.4:c.3725-74G= (RTEL1) NP_116575.3:n.3725-74G=
NR_037882.1:n.4649+54G= (RTEL1-TNFRSF6B)
NM_001283009.2:c.3822+54G= (RTEL1) MANE Select NP_001269938.1:n.3822+54G=
NM_016434.4:c.3653-74G= (RTEL1) NP_057518.1:n.3653-74G=
NM_032957.5:c.3725-74G= (RTEL1) NP_116575.3:n.3725-74G=