Canonical Allele Identifier: CA746520522

Gene: RTEL1-TNFRSF6B RTEL1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63694274G>A , CM000682.2:g.63694274G>A	GRCh38
NC_000020.10:g.62325627G>A , CM000682.1:g.62325627G>A	GRCh37
NC_000020.9:g.61796071G>A	NCBI36
NG_033901.1:g.41465G>A
NG_046961.1:g.2624G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697815.1:n.1740-98G>A (RTEL1-TNFRSF6B)
ENST00000508582.7:c.3065-98G>A (RTEL1)	ENSP00000424307.2:n.3065-98G>A
ENST00000318100.9:c.2324-98G>A (RTEL1)	ENSP00000322287.5:n.2324-98G>A
ENST00000360203.11:c.2993-98G>A (RTEL1) MANE Select	ENSP00000353332.5:n.2993-98G>A
ENST00000482936.6:c.2993-102G>A (RTEL1)	ENSP00000457868.2:n.2993-102G>A
ENST00000496281.2:n.3004-98G>A (RTEL1-TNFRSF6B)
ENST00000318100.8:c.2324-98G>A (RTEL1)	ENSP00000322287.5:n.2324-98G>A
ENST00000360203.9:c.2993-98G>A (RTEL1)	ENSP00000353332.5:n.2993-98G>A
ENST00000370003.2:c.728-98G>A (RTEL1)	ENSP00000359020.1:n.728-98G>A
ENST00000370018.7:c.2993-98G>A (RTEL1)	ENSP00000359035.3:n.2993-98G>A
ENST00000480273.5:n.3078-98G>A (RTEL1-TNFRSF6B)
ENST00000482936.5:c.2993-98G>A (RTEL1-TNFRSF6B)	ENSP00000457868.1:n.2993-98G>A
ENST00000492259.6:c.*595-98G>A (RTEL1-TNFRSF6B)	ENSP00000457428.1:n.*595-98G>A
ENST00000496281.1:n.2475-98G>A (RTEL1-TNFRSF6B)
ENST00000496816.5:c.872-45G>A (RTEL1)	ENSP00000425576.1:n.872-45G>A
ENST00000508582.6:c.3065-98G>A (RTEL1)	ENSP00000424307.2:n.3065-98G>A
NM_001283009.1:c.2993-98G>A (RTEL1)	NP_001269938.1:n.2993-98G>A
NM_001283010.1:c.2324-98G>A (RTEL1)	NP_001269939.1:n.2324-98G>A
NM_016434.3:c.2993-98G>A (RTEL1)	NP_057518.1:n.2993-98G>A
NM_032957.4:c.3065-98G>A (RTEL1)	NP_116575.3:n.3065-98G>A
NR_037882.1:n.3820-98G>A (RTEL1-TNFRSF6B)
NM_001283009.2:c.2993-98G>A (RTEL1) MANE Select	NP_001269938.1:n.2993-98G>A
NM_016434.4:c.2993-98G>A (RTEL1)	NP_057518.1:n.2993-98G>A
NM_032957.5:c.3065-98G>A (RTEL1)	NP_116575.3:n.3065-98G>A