Canonical Allele Identifier: CA364288530

Gene: RSPH9 POLR1C

Linked Data

• MyVariant Identifiers: chr6:g.43618170T>A (hg19) ; chr6:g.43650433T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43650433T>A , CM000668.2:g.43650433T>A	GRCh38
NC_000006.11:g.43618170T>A , CM000668.1:g.43618170T>A	GRCh37
NC_000006.10:g.43726148T>A	NCBI36
NG_023436.1:g.10404T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372163.5:c.286T>A (RSPH9) MANE Select	ENSP00000361236.4:p.Ser96Thr
ENST00000372163.4:c.286T>A (RSPH9)	ENSP00000361236.4:p.Ser96Thr
ENST00000372165.8:c.286T>A (RSPH9)	ENSP00000361238.4:p.Ser96Thr
NM_001193341.1:c.286T>A (RSPH9)	NP_001180270.1:p.Ser96Thr
NM_152732.4:c.286T>A (RSPH9)	NP_689945.2:p.Ser96Thr
XM_005248901.2:c.286T>A (RSPH9)	XP_005248958.1:p.Ser96Thr
XM_006715014.1:c.227+5108T>A (RSPH9)	XP_006715077.1:n.227+5108T>A
XM_011514356.1:c.286T>A (RSPH9)	XP_011512658.1:p.Ser96Thr
XR_926099.1:n.321T>A (RSPH9)
XM_005248901.3:c.286T>A (RSPH9)	XP_005248958.1:p.Ser96Thr
XR_002956268.1:n.328T>A (RSPH9)
XR_002956269.1:n.296+5108T>A (RSPH9)
XR_926099.2:n.328T>A (RSPH9)
NM_152732.5:c.286T>A (RSPH9) MANE Select	NP_689945.2:p.Ser96Thr
NM_001193341.2:c.286T>A (RSPH9)	NP_001180270.1:p.Ser96Thr
NM_001318876.2:c.945+121162T>A (POLR1C)	NP_001305805.1:n.945+121162T>A