Canonical Allele Identifier: CA409671932

Gene: RTEL1 RTEL1-TNFRSF6B

Linked Data

• gnomAD v4: 20-63672566-C-T
• MyVariant Identifiers: chr20:g.62303919C>T (hg19) ; chr20:g.63672566C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63672566C>T , CM000682.2:g.63672566C>T	GRCh38
NC_000020.10:g.62303919C>T , CM000682.1:g.62303919C>T	GRCh37
NC_000020.9:g.61774363C>T	NCBI36
NG_033901.1:g.19757C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425905.7:n.384C>T (RTEL1)
ENST00000425905.6:c.384C>T (RTEL1)
ENST00000508582.7:c.782C>T (RTEL1)	ENSP00000424307.2:p.Ala261Val
ENST00000684971.1:n.1141C>T (RTEL1)
ENST00000686756.1:n.1028C>T (RTEL1)
ENST00000687123.1:n.540C>T (RTEL1)
ENST00000692658.1:n.1148C>T (RTEL1)
ENST00000692911.1:n.1437C>T (RTEL1)
ENST00000318100.9:c.41C>T (RTEL1)	ENSP00000322287.5:p.Ala14Val
ENST00000360203.11:c.710C>T (RTEL1) MANE Select	ENSP00000353332.5:p.Ala237Val
ENST00000482936.6:c.710C>T (RTEL1)	ENSP00000457868.2:p.Ala237Val
ENST00000318100.8:c.41C>T (RTEL1)	ENSP00000322287.5:p.Ala14Val
ENST00000356810.5:c.860C>T (RTEL1)	ENSP00000349265.4:p.Ala287Val
ENST00000360203.9:c.710C>T (RTEL1)	ENSP00000353332.5:p.Ala237Val
ENST00000370018.7:c.710C>T (RTEL1)	ENSP00000359035.3:p.Ala237Val
ENST00000463361.1:n.407C>T (RTEL1)
ENST00000482936.5:c.710C>T (RTEL1-TNFRSF6B)	ENSP00000457868.1:p.Ala237Val
ENST00000492259.6:c.710C>T (RTEL1-TNFRSF6B)	ENSP00000457428.1:p.Ala237Val
ENST00000508582.6:c.782C>T (RTEL1)	ENSP00000424307.2:p.Ala261Val
NM_001283009.1:c.710C>T (RTEL1)	NP_001269938.1:p.Ala237Val
NM_001283010.1:c.41C>T (RTEL1)	NP_001269939.1:p.Ala14Val
NM_016434.3:c.710C>T (RTEL1)	NP_057518.1:p.Ala237Val
NM_032957.4:c.782C>T (RTEL1)	NP_116575.3:p.Ala261Val
NR_037882.1:n.1537C>T (RTEL1-TNFRSF6B)
NM_001283009.2:c.710C>T (RTEL1) MANE Select	NP_001269938.1:p.Ala237Val
NM_016434.4:c.710C>T (RTEL1)	NP_057518.1:p.Ala237Val
NM_032957.5:c.782C>T (RTEL1)	NP_116575.3:p.Ala261Val