Canonical Allele Identifier: CA9964109

Gene: RTEL1 RTEL1-TNFRSF6B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63661285G>A , CM000682.2:g.63661285G>A	GRCh38
NC_000020.10:g.62292638G>A , CM000682.1:g.62292638G>A	GRCh37
NC_000020.9:g.61763082G>A	NCBI36
NG_033901.1:g.8476G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001283009.2:c.103-13G>A (RTEL1) MANE Select	NP_001269938.1:n.103-13G>A
ENST00000360203.11:c.103-13G>A (RTEL1) MANE Select	ENSP00000353332.5:n.103-13G>A
NM_001283009.1:c.103-13G>A (RTEL1)	NP_001269938.1:n.103-13G>A
NM_001283010.1:c.-567-13G>A (RTEL1)	NP_001269939.1:n.-567-13G>A
NM_016434.3:c.103-13G>A (RTEL1)	NP_057518.1:n.103-13G>A
NM_016434.4:c.103-13G>A (RTEL1)	NP_057518.1:n.103-13G>A
NM_032957.4:c.103-13G>A (RTEL1)	NP_116575.3:n.103-13G>A
NM_032957.5:c.103-13G>A (RTEL1)	NP_116575.3:n.103-13G>A
NR_037882.1:n.930-13G>A (RTEL1-TNFRSF6B)
ENST00000318100.8:c.-567-13G>A (RTEL1)	ENSP00000322287.5:n.-567-13G>A
ENST00000318100.9:c.-567-13G>A (RTEL1)	ENSP00000322287.5:n.-567-13G>A
ENST00000356810.5:c.103-13G>A (RTEL1)	ENSP00000349265.4:n.103-13G>A
ENST00000360203.9:c.103-13G>A (RTEL1)	ENSP00000353332.5:n.103-13G>A
ENST00000370018.7:c.103-13G>A (RTEL1)	ENSP00000359035.3:n.103-13G>A
ENST00000469728.5:n.567-13G>A (RTEL1)
ENST00000482936.5:c.103-13G>A (RTEL1-TNFRSF6B)	ENSP00000457868.1:n.103-13G>A
ENST00000482936.6:c.103-13G>A (RTEL1)	ENSP00000457868.2:n.103-13G>A
ENST00000488316.1:n.357-13G>A (RTEL1)
ENST00000488316.2:n.373-13G>A (RTEL1)
ENST00000492259.6:c.103-13G>A (RTEL1-TNFRSF6B)	ENSP00000457428.1:n.103-13G>A
ENST00000508582.6:c.103-13G>A (RTEL1)	ENSP00000424307.2:n.103-13G>A
ENST00000508582.7:c.103-13G>A (RTEL1)	ENSP00000424307.2:n.103-13G>A
ENST00000646389.1:c.103-13G>A (RTEL1)	ENSP00000494280.1:n.103-13G>A
ENST00000684971.1:n.428-13G>A (RTEL1)
ENST00000686756.1:n.421-13G>A (RTEL1)
ENST00000692658.1:n.435-13G>A (RTEL1)
ENST00000692911.1:n.830-13G>A (RTEL1)