LDH info

Canonical Allele Identifier: CA14782107
Gene: RTEL1 HGNC NCBI
RTEL1-TNFRSF6B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4809219

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63671762C>A , CM000682.2:g.63671762C>A GRCh38
NC_000020.10:g.62303115C>A , CM000682.1:g.62303115C>A GRCh37
NC_000020.9:g.61773559C>A NCBI36
NG_033901.1:g.18953C>A

Transcript Alleles

HGVS Amino-acid change
NM_001283009.1:c.700-794C>A (RTEL1) VV NP_001269938.1:p.=
NM_001283010.1:c.31-794C>A (RTEL1) VV NP_001269939.1:p.=
NM_016434.3:c.700-794C>A (RTEL1) VV NP_057518.1:p.=
NM_032957.4:c.772-794C>A (RTEL1) VV NP_116575.3:p.=
NR_037882.1:n.1527-794C>A (RTEL1-TNFRSF6B)
NM_001283009.2:c.700-794C>A (RTEL1) VV NP_001269938.1:p.=
NM_016434.4:c.700-794C>A (RTEL1) VV NP_057518.1:p.=
NM_032957.5:c.772-794C>A (RTEL1) VV NP_116575.3:p.=
ENST00000318100.8:c.31-794C>A ENSP00000322287.5:p.=
ENST00000356810.5:c.850-794C>A ENSP00000349265.4:p.=
ENST00000360203.9:c.700-794C>A ENSP00000353332.5:p.=
ENST00000370018.7:c.700-794C>A ENSP00000359035.3:p.=
ENST00000463361.1:n.397-794C>A
ENST00000482936.5:n.700-794C>A ENSP00000457868.1:p.=
ENST00000492259.6:c.700-794C>A ENSP00000457428.1:p.=
ENST00000508582.6:c.772-794C>A ENSP00000424307.2:p.=