Canonical Allele Identifier: CA452983228
Community Standard Title: NM_031924.8(RSPH3):c.-418C>G
Gene: RSPH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158999968G>C , CM000668.2:g.158999968G>C GRCh38
NC_000006.11:g.159421000G>C , CM000668.1:g.159421000G>C GRCh37
NC_000006.10:g.159340988G>C NCBI36
NG_051819.1:g.5220C>G

Transcript Alleles

HGVS Amino-acid Change
NM_031924.8:c.-418C>G MANE Select NP_114130.4:n.-418C>G
ENST00000367069.7:c.-418C>G MANE Select ENSP00000356036.1:n.-418C>G
NM_001346418.1:c.9C>G NP_001333347.1:p.Val3=
NM_031924.4:c.9C>G NP_114130.3:p.Val3=
NM_031924.5:c.9C>G NP_114130.3:p.Val3=
NM_031924.6:c.9C>G NP_114130.3:p.Val3=
NR_144434.1:n.220C>G
ENST00000252655.1:c.9C>G ENSP00000252655.1:p.Val3=
ENST00000367069.6:c.-418C>G ENSP00000356036.1:n.-418C>G
XM_005267153.3:c.9C>G XP_005267210.1:p.Val3=
XR_001743668.2:n.459C>G
XR_001743669.2:n.459C>G
XR_001743670.2:n.459C>G
XR_245553.2:n.465C>G