Canonical Allele Identifier: CA2374928172

Gene: RTEL1 RTEL1-TNFRSF6B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63685277C= , CM000682.2:g.63685277C=	GRCh38
NC_000020.10:g.62316630C= , CM000682.1:g.62316630C=	GRCh37
NC_000020.9:g.61787074C=	NCBI36
NG_033901.1:g.32468C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001283009.2:c.1192-246C= (RTEL1) MANE Select	NP_001269938.1:n.1192-246C=
ENST00000360203.11:c.1192-246C= (RTEL1) MANE Select	ENSP00000353332.5:n.1192-246C=
NM_001283009.1:c.1192-246C= (RTEL1)	NP_001269938.1:n.1192-246C=
NM_001283010.1:c.523-246C= (RTEL1)	NP_001269939.1:n.523-246C=
NM_016434.3:c.1192-246C= (RTEL1)	NP_057518.1:n.1192-246C=
NM_016434.4:c.1192-246C= (RTEL1)	NP_057518.1:n.1192-246C=
NM_032957.4:c.1264-246C= (RTEL1)	NP_116575.3:n.1264-246C=
NM_032957.5:c.1264-246C= (RTEL1)	NP_116575.3:n.1264-246C=
NR_037882.1:n.2019-246C= (RTEL1-TNFRSF6B)
ENST00000318100.8:c.523-246C= (RTEL1)	ENSP00000322287.5:n.523-246C=
ENST00000318100.9:c.523-246C= (RTEL1)	ENSP00000322287.5:n.523-246C=
ENST00000360203.9:c.1192-246C= (RTEL1)	ENSP00000353332.5:n.1192-246C=
ENST00000370018.7:c.1192-246C= (RTEL1)	ENSP00000359035.3:n.1192-246C=
ENST00000425905.6:c.866-246C= (RTEL1)
ENST00000425905.7:n.866-246C= (RTEL1)
ENST00000482936.5:c.1192-246C= (RTEL1-TNFRSF6B)	ENSP00000457868.1:n.1192-246C=
ENST00000482936.6:c.1192-246C= (RTEL1)	ENSP00000457868.2:n.1192-246C=
ENST00000492259.6:c.1276-246C= (RTEL1-TNFRSF6B)	ENSP00000457428.1:n.1276-246C=
ENST00000508582.6:c.1264-246C= (RTEL1)	ENSP00000424307.2:n.1264-246C=
ENST00000508582.7:c.1264-246C= (RTEL1)	ENSP00000424307.2:n.1264-246C=
ENST00000647249.1:n.123-246C= (RTEL1)
ENST00000687123.1:n.1022-246C= (RTEL1)