Canonical Allele Identifier: CA1624619296

Gene: RSPH9 POLR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43650511G= , CM000668.2:g.43650511G=	GRCh38
NC_000006.11:g.43618248G= , CM000668.1:g.43618248G=	GRCh37
NC_000006.10:g.43726226G=	NCBI36
NG_023436.1:g.10482G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372163.5:c.364G= (RSPH9) MANE Select	ENSP00000361236.4:p.Gly122=
ENST00000372163.4:c.364G= (RSPH9)	ENSP00000361236.4:p.Gly122=
ENST00000372165.8:c.364G= (RSPH9)	ENSP00000361238.4:p.Gly122=
NM_001193341.1:c.364G= (RSPH9)	NP_001180270.1:p.Gly122=
NM_152732.4:c.364G= (RSPH9)	NP_689945.2:p.Gly122=
XM_005248901.2:c.364G= (RSPH9)	XP_005248958.1:p.Gly122=
XM_006715014.1:c.228-5051G= (RSPH9)	XP_006715077.1:n.228-5051G=
XM_011514356.1:c.364G= (RSPH9)	XP_011512658.1:p.Gly122=
XR_926099.1:n.399G= (RSPH9)
XM_005248901.3:c.364G= (RSPH9)	XP_005248958.1:p.Gly122=
XR_002956268.1:n.406G= (RSPH9)
XR_002956269.1:n.297-5051G= (RSPH9)
XR_926099.2:n.406G= (RSPH9)
NM_152732.5:c.364G= (RSPH9) MANE Select	NP_689945.2:p.Gly122=
NM_001193341.2:c.364G= (RSPH9)	NP_001180270.1:p.Gly122=
NM_001318876.2:c.945+121240G= (POLR1C)	NP_001305805.1:n.945+121240G=