Canonical Allele Identifier: CA14824472

Gene: RTEL1 RTEL1-TNFRSF6B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63667320C>G , CM000682.2:g.63667320C>G	GRCh38
NC_000020.10:g.62298673C>G , CM000682.1:g.62298673C>G	GRCh37
NC_000020.9:g.61769117C>G	NCBI36
NG_033901.1:g.14511C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425905.7:n.289-149C>G (RTEL1)
ENST00000425905.6:c.289-149C>G (RTEL1)
ENST00000508582.7:c.687-149C>G (RTEL1)	ENSP00000424307.2:n.687-149C>G
ENST00000684971.1:n.1046-149C>G (RTEL1)
ENST00000686756.1:n.933-149C>G (RTEL1)
ENST00000687123.1:n.445-149C>G (RTEL1)
ENST00000692658.1:n.1053-149C>G (RTEL1)
ENST00000692911.1:n.1342-149C>G (RTEL1)
ENST00000318100.9:c.-55-149C>G (RTEL1)	ENSP00000322287.5:n.-55-149C>G
ENST00000360203.11:c.615-149C>G (RTEL1) MANE Select	ENSP00000353332.5:n.615-149C>G
ENST00000482936.6:c.615-149C>G (RTEL1)	ENSP00000457868.2:n.615-149C>G
ENST00000318100.8:c.-55-149C>G (RTEL1)	ENSP00000322287.5:n.-55-149C>G
ENST00000356810.5:c.765-149C>G (RTEL1)	ENSP00000349265.4:n.765-149C>G
ENST00000360203.9:c.615-149C>G (RTEL1)	ENSP00000353332.5:n.615-149C>G
ENST00000370018.7:c.615-149C>G (RTEL1)	ENSP00000359035.3:n.615-149C>G
ENST00000463361.1:n.312-149C>G (RTEL1)
ENST00000482936.5:c.615-149C>G (RTEL1-TNFRSF6B)	ENSP00000457868.1:n.615-149C>G
ENST00000492259.6:c.615-149C>G (RTEL1-TNFRSF6B)	ENSP00000457428.1:n.615-149C>G
ENST00000508582.6:c.687-149C>G (RTEL1)	ENSP00000424307.2:n.687-149C>G
NM_001283009.1:c.615-149C>G (RTEL1)	NP_001269938.1:n.615-149C>G
NM_001283010.1:c.-55-149C>G (RTEL1)	NP_001269939.1:n.-55-149C>G
NM_016434.3:c.615-149C>G (RTEL1)	NP_057518.1:n.615-149C>G
NM_032957.4:c.687-149C>G (RTEL1)	NP_116575.3:n.687-149C>G
NR_037882.1:n.1442-149C>G (RTEL1-TNFRSF6B)
NM_001283009.2:c.615-149C>G (RTEL1) MANE Select	NP_001269938.1:n.615-149C>G
NM_016434.4:c.615-149C>G (RTEL1)	NP_057518.1:n.615-149C>G
NM_032957.5:c.687-149C>G (RTEL1)	NP_116575.3:n.687-149C>G