Canonical Allele Identifier: CA2374920805

Gene: RTEL1 RTEL1-TNFRSF6B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63672570C= , CM000682.2:g.63672570C=	GRCh38
NC_000020.10:g.62303923C= , CM000682.1:g.62303923C=	GRCh37
NC_000020.9:g.61774367C=	NCBI36
NG_033901.1:g.19761C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425905.7:n.388C= (RTEL1)
ENST00000425905.6:c.388C= (RTEL1)
ENST00000508582.7:c.786C= (RTEL1)	ENSP00000424307.2:p.His262=
ENST00000684971.1:n.1145C= (RTEL1)
ENST00000686756.1:n.1032C= (RTEL1)
ENST00000687123.1:n.544C= (RTEL1)
ENST00000692658.1:n.1152C= (RTEL1)
ENST00000692911.1:n.1441C= (RTEL1)
ENST00000318100.9:c.45C= (RTEL1)	ENSP00000322287.5:p.His15=
ENST00000360203.11:c.714C= (RTEL1) MANE Select	ENSP00000353332.5:p.His238=
ENST00000482936.6:c.714C= (RTEL1)	ENSP00000457868.2:p.His238=
ENST00000318100.8:c.45C= (RTEL1)	ENSP00000322287.5:p.His15=
ENST00000356810.5:c.864C= (RTEL1)	ENSP00000349265.4:p.His288=
ENST00000360203.9:c.714C= (RTEL1)	ENSP00000353332.5:p.His238=
ENST00000370018.7:c.714C= (RTEL1)	ENSP00000359035.3:p.His238=
ENST00000463361.1:n.411C= (RTEL1)
ENST00000482936.5:c.714C= (RTEL1-TNFRSF6B)	ENSP00000457868.1:p.His238=
ENST00000492259.6:c.714C= (RTEL1-TNFRSF6B)	ENSP00000457428.1:p.His238=
ENST00000508582.6:c.786C= (RTEL1)	ENSP00000424307.2:p.His262=
NM_001283009.1:c.714C= (RTEL1)	NP_001269938.1:p.His238=
NM_001283010.1:c.45C= (RTEL1)	NP_001269939.1:p.His15=
NM_016434.3:c.714C= (RTEL1)	NP_057518.1:p.His238=
NM_032957.4:c.786C= (RTEL1)	NP_116575.3:p.His262=
NR_037882.1:n.1541C= (RTEL1-TNFRSF6B)
NM_001283009.2:c.714C= (RTEL1) MANE Select	NP_001269938.1:p.His238=
NM_016434.4:c.714C= (RTEL1)	NP_057518.1:p.His238=
NM_032957.5:c.786C= (RTEL1)	NP_116575.3:p.His262=