Canonical Allele Identifier: CA9966026
Gene: RTEL1-TNFRSF6B HGNC NCBI
RTEL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 540953
dbSNP Id: rs41306796

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63695145G>A , CM000682.2:g.63695145G>A GRCh38
NC_000020.10:g.62326498G>A , CM000682.1:g.62326498G>A GRCh37
NC_000020.9:g.61796942G>A NCBI36
NG_033901.1:g.42336G>A
NG_046961.1:g.3495G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697815.1:n.2170G>A (RTEL1-TNFRSF6B)
ENST00000508582.7:c.3495G>A (RTEL1) ENSP00000424307.2:p.Pro1165=
ENST00000318100.9:c.2754G>A (RTEL1) ENSP00000322287.5:p.Pro918=
ENST00000360203.11:c.3423G>A (RTEL1) MANE Select ENSP00000353332.5:p.Pro1141=
ENST00000496281.2:n.3434G>A (RTEL1-TNFRSF6B)
ENST00000318100.8:c.2754G>A (RTEL1) ENSP00000322287.5:p.Pro918=
ENST00000360203.9:c.3423G>A (RTEL1) ENSP00000353332.5:p.Pro1141=
ENST00000370003.2:c.1158G>A (RTEL1) ENSP00000359020.1:p.Pro386=
ENST00000370018.7:c.3423G>A (RTEL1) ENSP00000359035.3:p.Pro1141=
ENST00000480273.5:n.3508G>A (RTEL1-TNFRSF6B)
ENST00000482936.5:c.3423G>A (RTEL1-TNFRSF6B) ENSP00000457868.1:p.Pro1141=
ENST00000492259.6:c.*1025G>A (RTEL1-TNFRSF6B) ENSP00000457428.1:n.*1025G>A
ENST00000496281.1:n.2905G>A (RTEL1-TNFRSF6B)
ENST00000496816.5:c.1355G>A (RTEL1) ENSP00000425576.1:n.1355G>A
ENST00000508582.6:c.3495G>A (RTEL1) ENSP00000424307.2:p.Pro1165=
NM_001283009.1:c.3423G>A (RTEL1) NP_001269938.1:p.Pro1141=
NM_001283010.1:c.2754G>A (RTEL1) NP_001269939.1:p.Pro918=
NM_016434.3:c.3423G>A (RTEL1) NP_057518.1:p.Pro1141=
NM_032957.4:c.3495G>A (RTEL1) NP_116575.3:p.Pro1165=
NR_037882.1:n.4250G>A (RTEL1-TNFRSF6B)
NM_001283009.2:c.3423G>A (RTEL1) MANE Select NP_001269938.1:p.Pro1141=
NM_016434.4:c.3423G>A (RTEL1) NP_057518.1:p.Pro1141=
NM_032957.5:c.3495G>A (RTEL1) NP_116575.3:p.Pro1165=