Canonical Allele Identifier: CA511661091

Gene: RTEL1 RTEL1-TNFRSF6B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63690114A>G , CM000682.2:g.63690114A>G	GRCh38
NC_000020.10:g.62321467A>G , CM000682.1:g.62321467A>G	GRCh37
NC_000020.9:g.61791911A>G	NCBI36
NG_033901.1:g.37305A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001283009.2:c.2169A>G (RTEL1) MANE Select	NP_001269938.1:p.Gln723=
ENST00000360203.11:c.2169A>G (RTEL1) MANE Select	ENSP00000353332.5:p.Gln723=
NM_001283009.1:c.2169A>G (RTEL1)	NP_001269938.1:p.Gln723=
NM_001283010.1:c.1500A>G (RTEL1)	NP_001269939.1:p.Gln500=
NM_016434.3:c.2169A>G (RTEL1)	NP_057518.1:p.Gln723=
NM_016434.4:c.2169A>G (RTEL1)	NP_057518.1:p.Gln723=
NM_032957.4:c.2241A>G (RTEL1)	NP_116575.3:p.Gln747=
NM_032957.5:c.2241A>G (RTEL1)	NP_116575.3:p.Gln747=
NR_037882.1:n.2996A>G (RTEL1-TNFRSF6B)
ENST00000318100.8:c.1500A>G (RTEL1)	ENSP00000322287.5:p.Gln500=
ENST00000318100.9:c.1500A>G (RTEL1)	ENSP00000322287.5:p.Gln500=
ENST00000360203.9:c.2169A>G (RTEL1)	ENSP00000353332.5:p.Gln723=
ENST00000370003.2:c.-97A>G (RTEL1)	ENSP00000359020.1:n.-97A>G
ENST00000370018.7:c.2169A>G (RTEL1)	ENSP00000359035.3:p.Gln723=
ENST00000425905.5:c.348A>G (RTEL1)	ENSP00000388063.1:p.Gln116=
ENST00000425905.6:c.1696A>G (RTEL1)
ENST00000425905.7:n.1696A>G (RTEL1)
ENST00000480273.5:n.2254A>G (RTEL1-TNFRSF6B)
ENST00000482936.5:c.2169A>G (RTEL1-TNFRSF6B)	ENSP00000457868.1:p.Gln723=
ENST00000482936.6:c.2169A>G (RTEL1)	ENSP00000457868.2:p.Gln723=
ENST00000492259.6:c.2226-180A>G (RTEL1-TNFRSF6B)	ENSP00000457428.1:n.2226-180A>G
ENST00000496281.1:n.684A>G (RTEL1-TNFRSF6B)
ENST00000496281.2:n.1213A>G (RTEL1-TNFRSF6B)
ENST00000496816.5:c.48A>G (RTEL1)	ENSP00000425576.1:p.Gln16=
ENST00000508582.6:c.2241A>G (RTEL1)	ENSP00000424307.2:p.Gln747=
ENST00000508582.7:c.2241A>G (RTEL1)	ENSP00000424307.2:p.Gln747=
ENST00000687123.1:n.1825-30A>G (RTEL1)
ENST00000697814.1:n.480A>G (RTEL1)
ENST00000697815.1:n.128A>G (RTEL1-TNFRSF6B)