Canonical Allele Identifier: CA409681337

Gene: RTEL1 RTEL1-TNFRSF6B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63690803A>G , CM000682.2:g.63690803A>G	GRCh38
NC_000020.10:g.62322156A>G , CM000682.1:g.62322156A>G	GRCh37
NC_000020.9:g.61792600A>G	NCBI36
NG_033901.1:g.37994A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001283009.2:c.2414-2A>G (RTEL1) MANE Select	NP_001269938.1:n.2414-2A>G
ENST00000360203.11:c.2414-2A>G (RTEL1) MANE Select	ENSP00000353332.5:n.2414-2A>G
NM_001283009.1:c.2414-2A>G (RTEL1)	NP_001269938.1:n.2414-2A>G
NM_001283010.1:c.1745-2A>G (RTEL1)	NP_001269939.1:n.1745-2A>G
NM_016434.3:c.2414-2A>G (RTEL1)	NP_057518.1:n.2414-2A>G
NM_016434.4:c.2414-2A>G (RTEL1)	NP_057518.1:n.2414-2A>G
NM_032957.4:c.2486-2A>G (RTEL1)	NP_116575.3:n.2486-2A>G
NM_032957.5:c.2486-2A>G (RTEL1)	NP_116575.3:n.2486-2A>G
NR_037882.1:n.3241-2A>G (RTEL1-TNFRSF6B)
ENST00000318100.8:c.1745-2A>G (RTEL1)	ENSP00000322287.5:n.1745-2A>G
ENST00000318100.9:c.1745-2A>G (RTEL1)	ENSP00000322287.5:n.1745-2A>G
ENST00000360203.9:c.2414-2A>G (RTEL1)	ENSP00000353332.5:n.2414-2A>G
ENST00000370003.2:c.149-2A>G (RTEL1)	ENSP00000359020.1:n.149-2A>G
ENST00000370018.7:c.2414-2A>G (RTEL1)	ENSP00000359035.3:n.2414-2A>G
ENST00000425905.5:c.593-2A>G (RTEL1)	ENSP00000388063.1:n.593-2A>G
ENST00000425905.6:c.1941-2A>G (RTEL1)
ENST00000425905.7:n.1941-2A>G (RTEL1)
ENST00000480273.5:n.2499-2A>G (RTEL1-TNFRSF6B)
ENST00000482936.5:c.2414-2A>G (RTEL1-TNFRSF6B)	ENSP00000457868.1:n.2414-2A>G
ENST00000482936.6:c.2414-2A>G (RTEL1)	ENSP00000457868.2:n.2414-2A>G
ENST00000492259.6:c.*16-2A>G (RTEL1-TNFRSF6B)	ENSP00000457428.1:n.*16-2A>G
ENST00000496281.1:n.929-2A>G (RTEL1-TNFRSF6B)
ENST00000496281.2:n.1458-2A>G (RTEL1-TNFRSF6B)
ENST00000496816.5:c.293-2A>G (RTEL1)	ENSP00000425576.1:n.293-2A>G
ENST00000508582.6:c.2486-2A>G (RTEL1)	ENSP00000424307.2:n.2486-2A>G
ENST00000508582.7:c.2486-2A>G (RTEL1)	ENSP00000424307.2:n.2486-2A>G
ENST00000697815.1:n.373-2A>G (RTEL1-TNFRSF6B)