Canonical Allele Identifier: CA409657549
Community Standard Title: NM_001283009.2(RTEL1):c.72C>G (p.Tyr24Ter)
Gene: RTEL1 HGNC NCBI
RTEL1-TNFRSF6B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63659474C>G , CM000682.2:g.63659474C>G GRCh38
NC_000020.10:g.62290827C>G , CM000682.1:g.62290827C>G GRCh37
NC_000020.9:g.61761271C>G NCBI36
NG_033901.1:g.6665C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001283009.2:c.72C>G (RTEL1) MANE Select NP_001269938.1:p.Tyr24Ter
ENST00000360203.11:c.72C>G (RTEL1) MANE Select ENSP00000353332.5:p.Tyr24Ter
NM_001283009.1:c.72C>G (RTEL1) NP_001269938.1:p.Tyr24Ter
NM_001283010.1:c.-568+1015C>G (RTEL1) NP_001269939.1:n.-568+1015C>G
NM_016434.3:c.72C>G (RTEL1) NP_057518.1:p.Tyr24Ter
NM_016434.4:c.72C>G (RTEL1) NP_057518.1:p.Tyr24Ter
NM_032957.4:c.72C>G (RTEL1) NP_116575.3:p.Tyr24Ter
NM_032957.5:c.72C>G (RTEL1) NP_116575.3:p.Tyr24Ter
NR_037882.1:n.899C>G (RTEL1-TNFRSF6B)
ENST00000318100.8:c.-568+1015C>G (RTEL1) ENSP00000322287.5:n.-568+1015C>G
ENST00000318100.9:c.-568+1015C>G (RTEL1) ENSP00000322287.5:n.-568+1015C>G
ENST00000356810.5:c.72C>G (RTEL1) ENSP00000349265.4:p.Tyr24Ter
ENST00000360203.9:c.72C>G (RTEL1) ENSP00000353332.5:p.Tyr24Ter
ENST00000370018.7:c.72C>G (RTEL1) ENSP00000359035.3:p.Tyr24Ter
ENST00000469728.5:n.415C>G (RTEL1)
ENST00000482936.5:c.72C>G (RTEL1-TNFRSF6B) ENSP00000457868.1:p.Tyr24Ter
ENST00000482936.6:c.72C>G (RTEL1) ENSP00000457868.2:p.Tyr24Ter
ENST00000488316.1:n.326C>G (RTEL1)
ENST00000488316.2:n.342C>G (RTEL1)
ENST00000492259.6:c.72C>G (RTEL1-TNFRSF6B) ENSP00000457428.1:p.Tyr24Ter
ENST00000508582.6:c.72C>G (RTEL1) ENSP00000424307.2:p.Tyr24Ter
ENST00000508582.7:c.72C>G (RTEL1) ENSP00000424307.2:p.Tyr24Ter
ENST00000646389.1:c.72C>G (RTEL1) ENSP00000494280.1:p.Tyr24Ter
ENST00000684971.1:n.397C>G (RTEL1)
ENST00000686756.1:n.390C>G (RTEL1)
ENST00000692658.1:n.404C>G (RTEL1)
ENST00000692911.1:n.799C>G (RTEL1)