Canonical Allele Identifier: CA366286110
Community Standard Title: NM_031924.8(RSPH3):c.-417A>T
Gene: RSPH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158999967T>A , CM000668.2:g.158999967T>A GRCh38
NC_000006.11:g.159420999T>A , CM000668.1:g.159420999T>A GRCh37
NC_000006.10:g.159340987T>A NCBI36
NG_051819.1:g.5221A>T

Transcript Alleles

HGVS Amino-acid Change
NM_031924.8:c.-417A>T MANE Select NP_114130.4:n.-417A>T
ENST00000367069.7:c.-417A>T MANE Select ENSP00000356036.1:n.-417A>T
NM_001346418.1:c.10A>T NP_001333347.1:p.Lys4Ter
NM_031924.4:c.10A>T NP_114130.3:p.Lys4Ter
NM_031924.5:c.10A>T NP_114130.3:p.Lys4Ter
NM_031924.6:c.10A>T NP_114130.3:p.Lys4Ter
NR_144434.1:n.221A>T
ENST00000252655.1:c.10A>T ENSP00000252655.1:p.Lys4Ter
ENST00000367069.6:c.-417A>T ENSP00000356036.1:n.-417A>T
XM_005267153.3:c.10A>T XP_005267210.1:p.Lys4Ter
XR_001743668.2:n.460A>T
XR_001743669.2:n.460A>T
XR_001743670.2:n.460A>T
XR_245553.2:n.466A>T