Canonical Allele Identifier: CA1088411848
Gene: RSPH9 HGNC NCBI
POLR1C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43650348_43650349insCTTCTC , CM000668.2:g.43650348_43650349insCTTCTC GRCh38
NC_000006.11:g.43618085_43618086insCTTCTC , CM000668.1:g.43618085_43618086insCTTCTC GRCh37
NC_000006.10:g.43726063_43726064insCTTCTC NCBI36
NG_023436.1:g.10319_10320insCTTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000372163.5:c.228-27_228-26insCTTCTC (RSPH9) MANE Select ENSP00000361236.4:n.228-27_228-26insCTTCTC
ENST00000372163.4:c.228-27_228-26insCTTCTC (RSPH9) ENSP00000361236.4:n.228-27_228-26insCTTCTC
ENST00000372165.8:c.228-27_228-26insCTTCTC (RSPH9) ENSP00000361238.4:n.228-27_228-26insCTTCTC
NM_001193341.1:c.228-27_228-26insCTTCTC (RSPH9) NP_001180270.1:n.228-27_228-26insCTTCTC
NM_152732.4:c.228-27_228-26insCTTCTC (RSPH9) NP_689945.2:n.228-27_228-26insCTTCTC
XM_005248901.2:c.228-27_228-26insCTTCTC (RSPH9) XP_005248958.1:n.228-27_228-26insCTTCTC
XM_006715014.1:c.227+5023_227+5024insCTTCTC (RSPH9) XP_006715077.1:n.227+5023_227+5024insCTTCTC
XM_011514356.1:c.228-27_228-26insCTTCTC (RSPH9) XP_011512658.1:n.228-27_228-26insCTTCTC
XR_926099.1:n.263-27_263-26insCTTCTC (RSPH9)
XM_005248901.3:c.228-27_228-26insCTTCTC (RSPH9) XP_005248958.1:n.228-27_228-26insCTTCTC
XR_002956268.1:n.270-27_270-26insCTTCTC (RSPH9)
XR_002956269.1:n.296+5023_296+5024insCTTCTC (RSPH9)
XR_926099.2:n.270-27_270-26insCTTCTC (RSPH9)
NM_152732.5:c.228-27_228-26insCTTCTC (RSPH9) MANE Select NP_689945.2:n.228-27_228-26insCTTCTC
NM_001193341.2:c.228-27_228-26insCTTCTC (RSPH9) NP_001180270.1:n.228-27_228-26insCTTCTC
NM_001318876.2:c.945+121077_945+121078insCTTCTC (POLR1C) NP_001305805.1:n.945+121077_945+121078insCTTCTC