Canonical Allele Identifier: CA317495730

Gene: RTEL1 RTEL1-TNFRSF6B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63673746A>G , CM000682.2:g.63673746A>G	GRCh38
NC_000020.10:g.62305099A>G , CM000682.1:g.62305099A>G	GRCh37
NC_000020.9:g.61775543A>G	NCBI36
NG_033901.1:g.20937A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001283009.2:c.766-194A>G (RTEL1) MANE Select	NP_001269938.1:n.766-194A>G
ENST00000360203.11:c.766-194A>G (RTEL1) MANE Select	ENSP00000353332.5:n.766-194A>G
NM_001283009.1:c.766-194A>G (RTEL1)	NP_001269938.1:n.766-194A>G
NM_001283010.1:c.97-194A>G (RTEL1)	NP_001269939.1:n.97-194A>G
NM_016434.3:c.766-194A>G (RTEL1)	NP_057518.1:n.766-194A>G
NM_016434.4:c.766-194A>G (RTEL1)	NP_057518.1:n.766-194A>G
NM_032957.4:c.838-194A>G (RTEL1)	NP_116575.3:n.838-194A>G
NM_032957.5:c.838-194A>G (RTEL1)	NP_116575.3:n.838-194A>G
NR_037882.1:n.1593-194A>G (RTEL1-TNFRSF6B)
ENST00000318100.8:c.97-194A>G (RTEL1)	ENSP00000322287.5:n.97-194A>G
ENST00000318100.9:c.97-194A>G (RTEL1)	ENSP00000322287.5:n.97-194A>G
ENST00000356810.5:c.916-194A>G (RTEL1)	ENSP00000349265.4:n.916-194A>G
ENST00000360203.9:c.766-194A>G (RTEL1)	ENSP00000353332.5:n.766-194A>G
ENST00000370018.7:c.766-194A>G (RTEL1)	ENSP00000359035.3:n.766-194A>G
ENST00000425905.6:c.440-194A>G (RTEL1)
ENST00000425905.7:n.440-194A>G (RTEL1)
ENST00000463361.1:n.463-194A>G (RTEL1)
ENST00000482936.5:c.766-194A>G (RTEL1-TNFRSF6B)	ENSP00000457868.1:n.766-194A>G
ENST00000482936.6:c.766-194A>G (RTEL1)	ENSP00000457868.2:n.766-194A>G
ENST00000492259.6:c.766-194A>G (RTEL1-TNFRSF6B)	ENSP00000457428.1:n.766-194A>G
ENST00000508582.6:c.838-194A>G (RTEL1)	ENSP00000424307.2:n.838-194A>G
ENST00000508582.7:c.838-194A>G (RTEL1)	ENSP00000424307.2:n.838-194A>G
ENST00000684971.1:n.1197-194A>G (RTEL1)
ENST00000686756.1:n.1084-194A>G (RTEL1)
ENST00000687123.1:n.596-194A>G (RTEL1)
ENST00000692658.1:n.1204-194A>G (RTEL1)
ENST00000692911.1:n.1493-194A>G (RTEL1)