Canonical Allele Identifier: CA9964644

Gene: RTEL1 RTEL1-TNFRSF6B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63680717C>G , CM000682.2:g.63680717C>G	GRCh38
NC_000020.10:g.62312070C>G , CM000682.1:g.62312070C>G	GRCh37
NC_000020.9:g.61782514C>G	NCBI36
NG_033901.1:g.27908C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001283009.2:c.1189C>G (RTEL1) MANE Select	NP_001269938.1:p.Gln397Glu
ENST00000360203.11:c.1189C>G (RTEL1) MANE Select	ENSP00000353332.5:p.Gln397Glu
NM_001283009.1:c.1189C>G (RTEL1)	NP_001269938.1:p.Gln397Glu
NM_001283010.1:c.520C>G (RTEL1)	NP_001269939.1:p.Gln174Glu
NM_016434.3:c.1189C>G (RTEL1)	NP_057518.1:p.Gln397Glu
NM_016434.4:c.1189C>G (RTEL1)	NP_057518.1:p.Gln397Glu
NM_032957.4:c.1261C>G (RTEL1)	NP_116575.3:p.Gln421Glu
NM_032957.5:c.1261C>G (RTEL1)	NP_116575.3:p.Gln421Glu
NR_037882.1:n.2016C>G (RTEL1-TNFRSF6B)
ENST00000318100.8:c.520C>G (RTEL1)	ENSP00000322287.5:p.Gln174Glu
ENST00000318100.9:c.520C>G (RTEL1)	ENSP00000322287.5:p.Gln174Glu
ENST00000360203.9:c.1189C>G (RTEL1)	ENSP00000353332.5:p.Gln397Glu
ENST00000370018.7:c.1189C>G (RTEL1)	ENSP00000359035.3:p.Gln397Glu
ENST00000425905.6:c.863C>G (RTEL1)
ENST00000425905.7:n.863C>G (RTEL1)
ENST00000482936.5:c.1189C>G (RTEL1-TNFRSF6B)	ENSP00000457868.1:p.Gln397Glu
ENST00000482936.6:c.1189C>G (RTEL1)	ENSP00000457868.2:p.Gln397Glu
ENST00000492259.6:c.1273C>G (RTEL1-TNFRSF6B)	ENSP00000457428.1:p.Gln425Glu
ENST00000508582.6:c.1261C>G (RTEL1)	ENSP00000424307.2:p.Gln421Glu
ENST00000508582.7:c.1261C>G (RTEL1)	ENSP00000424307.2:p.Gln421Glu
ENST00000684971.1:n.1620C>G (RTEL1)
ENST00000687123.1:n.1019C>G (RTEL1)