Canonical Allele Identifier: CA409671923

Gene: RTEL1 RTEL1-TNFRSF6B

Linked Data

• MyVariant Identifiers: chr20:g.62303917A>C (hg19) ; chr20:g.63672564A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63672564A>C , CM000682.2:g.63672564A>C	GRCh38
NC_000020.10:g.62303917A>C , CM000682.1:g.62303917A>C	GRCh37
NC_000020.9:g.61774361A>C	NCBI36
NG_033901.1:g.19755A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425905.7:n.382A>C (RTEL1)
ENST00000425905.6:c.382A>C (RTEL1)
ENST00000508582.7:c.780A>C (RTEL1)	ENSP00000424307.2:p.Arg260Ser
ENST00000684971.1:n.1139A>C (RTEL1)
ENST00000686756.1:n.1026A>C (RTEL1)
ENST00000687123.1:n.538A>C (RTEL1)
ENST00000692658.1:n.1146A>C (RTEL1)
ENST00000692911.1:n.1435A>C (RTEL1)
ENST00000318100.9:c.39A>C (RTEL1)	ENSP00000322287.5:p.Arg13Ser
ENST00000360203.11:c.708A>C (RTEL1) MANE Select	ENSP00000353332.5:p.Arg236Ser
ENST00000482936.6:c.708A>C (RTEL1)	ENSP00000457868.2:p.Arg236Ser
ENST00000318100.8:c.39A>C (RTEL1)	ENSP00000322287.5:p.Arg13Ser
ENST00000356810.5:c.858A>C (RTEL1)	ENSP00000349265.4:p.Arg286Ser
ENST00000360203.9:c.708A>C (RTEL1)	ENSP00000353332.5:p.Arg236Ser
ENST00000370018.7:c.708A>C (RTEL1)	ENSP00000359035.3:p.Arg236Ser
ENST00000463361.1:n.405A>C (RTEL1)
ENST00000482936.5:c.708A>C (RTEL1-TNFRSF6B)	ENSP00000457868.1:p.Arg236Ser
ENST00000492259.6:c.708A>C (RTEL1-TNFRSF6B)	ENSP00000457428.1:p.Arg236Ser
ENST00000508582.6:c.780A>C (RTEL1)	ENSP00000424307.2:p.Arg260Ser
NM_001283009.1:c.708A>C (RTEL1)	NP_001269938.1:p.Arg236Ser
NM_001283010.1:c.39A>C (RTEL1)	NP_001269939.1:p.Arg13Ser
NM_016434.3:c.708A>C (RTEL1)	NP_057518.1:p.Arg236Ser
NM_032957.4:c.780A>C (RTEL1)	NP_116575.3:p.Arg260Ser
NR_037882.1:n.1535A>C (RTEL1-TNFRSF6B)
NM_001283009.2:c.708A>C (RTEL1) MANE Select	NP_001269938.1:p.Arg236Ser
NM_016434.4:c.708A>C (RTEL1)	NP_057518.1:p.Arg236Ser
NM_032957.5:c.780A>C (RTEL1)	NP_116575.3:p.Arg260Ser