Canonical Allele Identifier: CA2374930407

Gene: RTEL1 RTEL1-TNFRSF6B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63689115G= , CM000682.2:g.63689115G=	GRCh38
NC_000020.10:g.62320468G= , CM000682.1:g.62320468G=	GRCh37
NC_000020.9:g.61790912G=	NCBI36
NG_033901.1:g.36306G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001283009.2:c.1861G= (RTEL1) MANE Select	NP_001269938.1:p.Ala621=
ENST00000360203.11:c.1861G= (RTEL1) MANE Select	ENSP00000353332.5:p.Ala621=
NM_001283009.1:c.1861G= (RTEL1)	NP_001269938.1:p.Ala621=
NM_001283010.1:c.1192G= (RTEL1)	NP_001269939.1:p.Ala398=
NM_016434.3:c.1861G= (RTEL1)	NP_057518.1:p.Ala621=
NM_016434.4:c.1861G= (RTEL1)	NP_057518.1:p.Ala621=
NM_032957.4:c.1933G= (RTEL1)	NP_116575.3:p.Ala645=
NM_032957.5:c.1933G= (RTEL1)	NP_116575.3:p.Ala645=
NR_037882.1:n.2688G= (RTEL1-TNFRSF6B)
ENST00000318100.8:c.1192G= (RTEL1)	ENSP00000322287.5:p.Ala398=
ENST00000318100.9:c.1192G= (RTEL1)	ENSP00000322287.5:p.Ala398=
ENST00000360203.9:c.1861G= (RTEL1)	ENSP00000353332.5:p.Ala621=
ENST00000370018.7:c.1861G= (RTEL1)	ENSP00000359035.3:p.Ala621=
ENST00000425905.5:c.187G= (RTEL1)	ENSP00000388063.1:p.Ala63=
ENST00000425905.6:c.1535G= (RTEL1)
ENST00000425905.7:n.1535G= (RTEL1)
ENST00000480273.5:n.1946G= (RTEL1-TNFRSF6B)
ENST00000482936.5:c.1861G= (RTEL1-TNFRSF6B)	ENSP00000457868.1:p.Ala621=
ENST00000482936.6:c.1861G= (RTEL1)	ENSP00000457868.2:p.Ala621=
ENST00000492259.6:c.1945G= (RTEL1-TNFRSF6B)	ENSP00000457428.1:p.Ala649=
ENST00000496281.1:n.155G= (RTEL1-TNFRSF6B)
ENST00000496281.2:n.684G= (RTEL1-TNFRSF6B)
ENST00000508582.6:c.1933G= (RTEL1)	ENSP00000424307.2:p.Ala645=
ENST00000508582.7:c.1933G= (RTEL1)	ENSP00000424307.2:p.Ala645=
ENST00000687123.1:n.1691G= (RTEL1)
ENST00000697814.1:n.51G= (RTEL1)