Canonical Allele Identifier: CA511662312

Gene: RTEL1-TNFRSF6B RTEL1

Linked Data

• MyVariant Identifiers: chr20:g.62326955T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63695602T>G , CM000682.2:g.63695602T>G	GRCh38
NC_000020.10:g.62326955T>G , CM000682.1:g.62326955T>G	GRCh37
NC_000020.9:g.61797399T>G	NCBI36
NG_033901.1:g.42793T>G
NG_046961.1:g.3952T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697815.1:n.2521T>G (RTEL1-TNFRSF6B)
ENST00000508582.7:c.3724+122T>G (RTEL1)	ENSP00000424307.2:n.3724+122T>G
ENST00000318100.9:c.2983+122T>G (RTEL1)	ENSP00000322287.5:n.2983+122T>G
ENST00000360203.11:c.3774T>G (RTEL1) MANE Select	ENSP00000353332.5:p.Pro1258=
ENST00000496281.2:n.3785T>G (RTEL1-TNFRSF6B)
ENST00000318100.8:c.2983+122T>G (RTEL1)	ENSP00000322287.5:n.2983+122T>G
ENST00000360203.9:c.3774T>G (RTEL1)	ENSP00000353332.5:p.Pro1258=
ENST00000370003.2:c.1509T>G (RTEL1)	ENSP00000359020.1:p.Pro503=
ENST00000370018.7:c.3652+122T>G (RTEL1)	ENSP00000359035.3:n.3652+122T>G
ENST00000480273.5:n.3737+122T>G (RTEL1-TNFRSF6B)
ENST00000482936.5:c.3774T>G (RTEL1-TNFRSF6B)	ENSP00000457868.1:p.Pro1258=
ENST00000492259.6:c.*1254+122T>G (RTEL1-TNFRSF6B)	ENSP00000457428.1:n.*1254+122T>G
ENST00000496281.1:n.3256T>G (RTEL1-TNFRSF6B)
ENST00000496816.5:c.1706T>G (RTEL1)	ENSP00000425576.1:n.1706T>G
ENST00000508582.6:c.3724+122T>G (RTEL1)	ENSP00000424307.2:n.3724+122T>G
NM_001283009.1:c.3774T>G (RTEL1)	NP_001269938.1:p.Pro1258=
NM_001283010.1:c.2983+122T>G (RTEL1)	NP_001269939.1:n.2983+122T>G
NM_016434.3:c.3652+122T>G (RTEL1)	NP_057518.1:n.3652+122T>G
NM_032957.4:c.3724+122T>G (RTEL1)	NP_116575.3:n.3724+122T>G
NR_037882.1:n.4601T>G (RTEL1-TNFRSF6B)
NM_001283009.2:c.3774T>G (RTEL1) MANE Select	NP_001269938.1:p.Pro1258=
NM_016434.4:c.3652+122T>G (RTEL1)	NP_057518.1:n.3652+122T>G
NM_032957.5:c.3724+122T>G (RTEL1)	NP_116575.3:n.3724+122T>G