Canonical Allele Identifier: CA1926337314

Gene: RNLS

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331772.9:c.701-1445T>G MANE Select	ENSP00000332530.4:n.701-1445T>G
ENST00000331772.8:c.701-1445T>G	ENSP00000332530.4:n.701-1445T>G
ENST00000371947.7:c.701-1445T>G	ENSP00000361015.3:n.701-1445T>G
ENST00000466945.5:n.684-1445T>G
NM_001031709.2:c.701-1445T>G	NP_001026879.2:n.701-1445T>G
NM_018363.3:c.701-1445T>G	NP_060833.1:n.701-1445T>G
XM_005269946.1:c.701-1445T>G	XP_005270003.1:n.701-1445T>G
XM_005269947.1:c.701-30580T>G	XP_005270004.1:n.701-30580T>G
XM_005269948.1:c.452-1445T>G	XP_005270005.1:n.452-1445T>G
XM_005269950.2:c.452-1445T>G	XP_005270007.1:n.452-1445T>G
XM_011539924.1:c.701-1445T>G	XP_011538226.1:n.701-1445T>G
XM_011539925.1:c.701-1445T>G	XP_011538227.1:n.701-1445T>G
XM_011539926.1:c.701-1445T>G	XP_011538228.1:n.701-1445T>G
XM_011539927.1:c.701-1445T>G	XP_011538229.1:n.701-1445T>G
XR_946176.1:n.315-53993A>C
XM_005269946.2:c.701-1445T>G	XP_005270003.1:n.701-1445T>G
XM_005269947.2:c.701-30580T>G	XP_005270004.1:n.701-30580T>G
XM_005269948.3:c.452-1445T>G	XP_005270005.1:n.452-1445T>G
XM_005269950.4:c.452-1445T>G	XP_005270007.1:n.452-1445T>G
XM_011539924.3:c.701-1445T>G	XP_011538226.1:n.701-1445T>G
XM_011539927.3:c.701-1445T>G	XP_011538229.1:n.701-1445T>G
XM_017016380.2:c.701-1445T>G	XP_016871869.1:n.701-1445T>G
XM_017016381.2:c.701-1445T>G	XP_016871870.1:n.701-1445T>G
XM_017016382.2:c.452-1445T>G	XP_016871871.1:n.452-1445T>G
XM_017016384.2:c.452-30580T>G	XP_016871873.1:n.452-30580T>G
XM_017016385.1:c.215-1445T>G	XP_016871874.1:n.215-1445T>G
XM_024448063.1:c.452-1445T>G	XP_024303831.1:n.452-1445T>G
XR_001747122.2:n.1991-1445T>G
XR_001747537.2:n.657-53993A>C
NM_001031709.3:c.701-1445T>G MANE Select	NP_001026879.2:n.701-1445T>G
NM_018363.4:c.701-1445T>G	NP_060833.1:n.701-1445T>G