Canonical Allele Identifier: CA211636620

Gene: RNLS

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.88285726A>T , CM000672.2:g.88285726A>T	GRCh38
NC_000010.10:g.90045483A>T , CM000672.1:g.90045483A>T	GRCh37
NC_000010.9:g.90035463A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331772.9:c.877-220T>A MANE Select	ENSP00000332530.4:n.877-220T>A
ENST00000331772.8:c.877-220T>A	ENSP00000332530.4:n.877-220T>A
ENST00000371947.7:c.877-10694T>A	ENSP00000361015.3:n.877-10694T>A
NM_001031709.2:c.877-220T>A	NP_001026879.2:n.877-220T>A
NM_018363.3:c.877-10694T>A	NP_060833.1:n.877-10694T>A
XM_005269946.1:c.*46-220T>A	XP_005270003.1:n.*46-220T>A
XM_005269947.1:c.701-220T>A	XP_005270004.1:n.701-220T>A
XM_005269948.1:c.628-220T>A	XP_005270005.1:n.628-220T>A
XM_005269950.2:c.628-10694T>A	XP_005270007.1:n.628-10694T>A
XM_011539924.1:c.877-10694T>A	XP_011538226.1:n.877-10694T>A
XM_011539925.1:c.877-10694T>A	XP_011538227.1:n.877-10694T>A
XR_946176.1:n.315-84353A>T
XM_005269946.2:c.*46-220T>A	XP_005270003.1:n.*46-220T>A
XM_005269947.2:c.701-220T>A	XP_005270004.1:n.701-220T>A
XM_005269948.3:c.628-220T>A	XP_005270005.1:n.628-220T>A
XM_005269950.4:c.628-10694T>A	XP_005270007.1:n.628-10694T>A
XM_011539924.3:c.877-10694T>A	XP_011538226.1:n.877-10694T>A
XM_017016380.2:c.877-10694T>A	XP_016871869.1:n.877-10694T>A
XM_017016382.2:c.628-10694T>A	XP_016871871.1:n.628-10694T>A
XM_017016384.2:c.452-220T>A	XP_016871873.1:n.452-220T>A
XM_017016385.1:c.391-220T>A	XP_016871874.1:n.391-220T>A
XM_024448063.1:c.*46-220T>A	XP_024303831.1:n.*46-220T>A
XR_001747122.2:n.2167-10694T>A
XR_001747537.2:n.657-84353A>T
NM_001031709.3:c.877-220T>A MANE Select	NP_001026879.2:n.877-220T>A
NM_018363.4:c.877-10694T>A	NP_060833.1:n.877-10694T>A