Canonical Allele Identifier: CA364288653

Gene: RSPH9 POLR1C

Linked Data

• dbSNP Id: rs1032347070
• gnomAD v3: 6-43650466-C-G
• gnomAD v4: 6-43650466-C-G
• MyVariant Identifiers: chr6:g.43618203C>G (hg19) ; chr6:g.43650466C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43650466C>G , CM000668.2:g.43650466C>G	GRCh38
NC_000006.11:g.43618203C>G , CM000668.1:g.43618203C>G	GRCh37
NC_000006.10:g.43726181C>G	NCBI36
NG_023436.1:g.10437C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372163.5:c.319C>G (RSPH9) MANE Select	ENSP00000361236.4:p.Pro107Ala
ENST00000372163.4:c.319C>G (RSPH9)	ENSP00000361236.4:p.Pro107Ala
ENST00000372165.8:c.319C>G (RSPH9)	ENSP00000361238.4:p.Pro107Ala
NM_001193341.1:c.319C>G (RSPH9)	NP_001180270.1:p.Pro107Ala
NM_152732.4:c.319C>G (RSPH9)	NP_689945.2:p.Pro107Ala
XM_005248901.2:c.319C>G (RSPH9)	XP_005248958.1:p.Pro107Ala
XM_006715014.1:c.228-5096C>G (RSPH9)	XP_006715077.1:n.228-5096C>G
XM_011514356.1:c.319C>G (RSPH9)	XP_011512658.1:p.Pro107Ala
XR_926099.1:n.354C>G (RSPH9)
XM_005248901.3:c.319C>G (RSPH9)	XP_005248958.1:p.Pro107Ala
XR_002956268.1:n.361C>G (RSPH9)
XR_002956269.1:n.297-5096C>G (RSPH9)
XR_926099.2:n.361C>G (RSPH9)
NM_152732.5:c.319C>G (RSPH9) MANE Select	NP_689945.2:p.Pro107Ala
NM_001193341.2:c.319C>G (RSPH9)	NP_001180270.1:p.Pro107Ala
NM_001318876.2:c.945+121195C>G (POLR1C)	NP_001305805.1:n.945+121195C>G