Canonical Allele Identifier: CA2374920800

Gene: RTEL1 RTEL1-TNFRSF6B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63672563G= , CM000682.2:g.63672563G=	GRCh38
NC_000020.10:g.62303916G= , CM000682.1:g.62303916G=	GRCh37
NC_000020.9:g.61774360G=	NCBI36
NG_033901.1:g.19754G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425905.7:n.381G= (RTEL1)
ENST00000425905.6:c.381G= (RTEL1)
ENST00000508582.7:c.779G= (RTEL1)	ENSP00000424307.2:p.Arg260=
ENST00000684971.1:n.1138G= (RTEL1)
ENST00000686756.1:n.1025G= (RTEL1)
ENST00000687123.1:n.537G= (RTEL1)
ENST00000692658.1:n.1145G= (RTEL1)
ENST00000692911.1:n.1434G= (RTEL1)
ENST00000318100.9:c.38G= (RTEL1)	ENSP00000322287.5:p.Arg13=
ENST00000360203.11:c.707G= (RTEL1) MANE Select	ENSP00000353332.5:p.Arg236=
ENST00000482936.6:c.707G= (RTEL1)	ENSP00000457868.2:p.Arg236=
ENST00000318100.8:c.38G= (RTEL1)	ENSP00000322287.5:p.Arg13=
ENST00000356810.5:c.857G= (RTEL1)	ENSP00000349265.4:p.Arg286=
ENST00000360203.9:c.707G= (RTEL1)	ENSP00000353332.5:p.Arg236=
ENST00000370018.7:c.707G= (RTEL1)	ENSP00000359035.3:p.Arg236=
ENST00000463361.1:n.404G= (RTEL1)
ENST00000482936.5:c.707G= (RTEL1-TNFRSF6B)	ENSP00000457868.1:p.Arg236=
ENST00000492259.6:c.707G= (RTEL1-TNFRSF6B)	ENSP00000457428.1:p.Arg236=
ENST00000508582.6:c.779G= (RTEL1)	ENSP00000424307.2:p.Arg260=
NM_001283009.1:c.707G= (RTEL1)	NP_001269938.1:p.Arg236=
NM_001283010.1:c.38G= (RTEL1)	NP_001269939.1:p.Arg13=
NM_016434.3:c.707G= (RTEL1)	NP_057518.1:p.Arg236=
NM_032957.4:c.779G= (RTEL1)	NP_116575.3:p.Arg260=
NR_037882.1:n.1534G= (RTEL1-TNFRSF6B)
NM_001283009.2:c.707G= (RTEL1) MANE Select	NP_001269938.1:p.Arg236=
NM_016434.4:c.707G= (RTEL1)	NP_057518.1:p.Arg236=
NM_032957.5:c.779G= (RTEL1)	NP_116575.3:p.Arg260=