Canonical Allele Identifier: CA1624619269

Gene: RSPH9 POLR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43650440T= , CM000668.2:g.43650440T=	GRCh38
NC_000006.11:g.43618177T= , CM000668.1:g.43618177T=	GRCh37
NC_000006.10:g.43726155T=	NCBI36
NG_023436.1:g.10411T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372163.5:c.293T= (RSPH9) MANE Select	ENSP00000361236.4:p.Val98=
ENST00000372163.4:c.293T= (RSPH9)	ENSP00000361236.4:p.Val98=
ENST00000372165.8:c.293T= (RSPH9)	ENSP00000361238.4:p.Val98=
NM_001193341.1:c.293T= (RSPH9)	NP_001180270.1:p.Val98=
NM_152732.4:c.293T= (RSPH9)	NP_689945.2:p.Val98=
XM_005248901.2:c.293T= (RSPH9)	XP_005248958.1:p.Val98=
XM_006715014.1:c.227+5115T= (RSPH9)	XP_006715077.1:n.227+5115T=
XM_011514356.1:c.293T= (RSPH9)	XP_011512658.1:p.Val98=
XR_926099.1:n.328T= (RSPH9)
XM_005248901.3:c.293T= (RSPH9)	XP_005248958.1:p.Val98=
XR_002956268.1:n.335T= (RSPH9)
XR_002956269.1:n.296+5115T= (RSPH9)
XR_926099.2:n.335T= (RSPH9)
NM_152732.5:c.293T= (RSPH9) MANE Select	NP_689945.2:p.Val98=
NM_001193341.2:c.293T= (RSPH9)	NP_001180270.1:p.Val98=
NM_001318876.2:c.945+121169T= (POLR1C)	NP_001305805.1:n.945+121169T=