Canonical Allele Identifier: CA9965638

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.63693160C>G , CM000682.2:g.63693160C>G	GRCh38
NC_000020.10:g.62324513C>G , CM000682.1:g.62324513C>G	GRCh37
NC_000020.9:g.61794957C>G	NCBI36
NG_033901.1:g.40351C>G
NG_046961.1:g.1510C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697815.1:n.1616C>G (RTEL1-TNFRSF6B)
ENST00000508582.7:c.2941C>G (RTEL1)	ENSP00000424307.2:p.Arg981Gly
ENST00000318100.9:c.2200C>G (RTEL1)	ENSP00000322287.5:p.Arg734Gly
ENST00000360203.11:c.2869C>G (RTEL1) MANE Select	ENSP00000353332.5:p.Arg957Gly
ENST00000482936.6:c.2869C>G (RTEL1)	ENSP00000457868.2:p.Arg957Gly
ENST00000496281.2:n.2880C>G (RTEL1-TNFRSF6B)
ENST00000318100.8:c.2200C>G (RTEL1)	ENSP00000322287.5:p.Arg734Gly
ENST00000360203.9:c.2869C>G (RTEL1)	ENSP00000353332.5:p.Arg957Gly
ENST00000370003.2:c.604C>G (RTEL1)	ENSP00000359020.1:p.Arg202Gly
ENST00000370018.7:c.2869C>G (RTEL1)	ENSP00000359035.3:p.Arg957Gly
ENST00000480273.5:n.2954C>G (RTEL1-TNFRSF6B)
ENST00000482936.5:c.2869C>G (RTEL1-TNFRSF6B)	ENSP00000457868.1:p.Arg957Gly
ENST00000492259.6:c.*471C>G (RTEL1-TNFRSF6B)	ENSP00000457428.1:n.*471C>G
ENST00000496281.1:n.2351C>G (RTEL1-TNFRSF6B)
ENST00000496816.5:c.748C>G (RTEL1)	ENSP00000425576.1:p.Arg250Gly
ENST00000508582.6:c.2941C>G (RTEL1)	ENSP00000424307.2:p.Arg981Gly
NM_001283009.1:c.2869C>G (RTEL1)	NP_001269938.1:p.Arg957Gly
NM_001283010.1:c.2200C>G (RTEL1)	NP_001269939.1:p.Arg734Gly
NM_016434.3:c.2869C>G (RTEL1)	NP_057518.1:p.Arg957Gly
NM_032957.4:c.2941C>G (RTEL1)	NP_116575.3:p.Arg981Gly
NR_037882.1:n.3696C>G (RTEL1-TNFRSF6B)
NM_001283009.2:c.2869C>G (RTEL1) MANE Select	NP_001269938.1:p.Arg957Gly
NM_016434.4:c.2869C>G (RTEL1)	NP_057518.1:p.Arg957Gly
NM_032957.5:c.2941C>G (RTEL1)	NP_116575.3:p.Arg981Gly