Canonical Allele Identifier: CA13198264
Gene: RNLS HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10887800

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.88316086A>G , CM000672.2:g.88316086A>G GRCh38
NC_000010.10:g.90075843A>G , CM000672.1:g.90075843A>G GRCh37
NC_000010.9:g.90065823A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001031709.2:c.701-1445T>C VV NP_001026879.2:p.=
NM_018363.3:c.701-1445T>C VV NP_060833.1:p.=
XM_005269946.1:c.701-1445T>C XP_005270003.1:p.=
XM_005269947.1:c.701-30580T>C XP_005270004.1:p.=
XM_005269948.1:c.452-1445T>C XP_005270005.1:p.=
XM_005269950.2:c.452-1445T>C XP_005270007.1:p.=
XM_011539924.1:c.701-1445T>C XP_011538226.1:p.=
XM_011539925.1:c.701-1445T>C XP_011538227.1:p.=
XM_011539926.1:c.701-1445T>C XP_011538228.1:p.=
XM_011539927.1:c.701-1445T>C XP_011538229.1:p.=
XR_946176.1:n.315-53993A>G
XM_005269946.2:c.701-1445T>C XP_005270003.1:p.=
XM_005269947.2:c.701-30580T>C XP_005270004.1:p.=
XM_005269948.3:c.452-1445T>C XP_005270005.1:p.=
XM_005269950.4:c.452-1445T>C XP_005270007.1:p.=
XM_011539924.3:c.701-1445T>C XP_011538226.1:p.=
XM_011539927.3:c.701-1445T>C XP_011538229.1:p.=
XM_017016380.2:c.701-1445T>C XP_016871869.1:p.=
XM_017016381.2:c.701-1445T>C XP_016871870.1:p.=
XM_017016382.2:c.452-1445T>C XP_016871871.1:p.=
XM_017016384.2:c.452-30580T>C XP_016871873.1:p.=
XM_017016385.1:c.215-1445T>C XP_016871874.1:p.=
XM_024448063.1:c.452-1445T>C XP_024303831.1:p.=
XR_001747122.2:n.1991-1445T>C
XR_001747537.2:n.657-53993A>G
NM_001031709.3:c.701-1445T>C VV MANE Preferred NP_001026879.2:p.=
ENST00000331772.8:c.701-1445T>C ENSP00000332530.4:p.=
ENST00000371947.7:c.701-1445T>C ENSP00000361015.3:p.=
ENST00000466945.5:n.684-1445T>C