Canonical Allele Identifier: CA452982692

Gene: RSPH3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158999560C>T , CM000668.2:g.158999560C>T	GRCh38
NC_000006.11:g.159420592C>T , CM000668.1:g.159420592C>T	GRCh37
NC_000006.10:g.159340580C>T	NCBI36
NG_051819.1:g.5628G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_031924.8:c.-10G>A MANE Select	NP_114130.4:n.-10G>A
ENST00000367069.7:c.-10G>A MANE Select	ENSP00000356036.1:n.-10G>A
NM_001346418.1:c.417G>A	NP_001333347.1:p.Gln139=
NM_031924.4:c.417G>A	NP_114130.3:p.Gln139=
NM_031924.5:c.417G>A	NP_114130.3:p.Gln139=
NM_031924.6:c.417G>A	NP_114130.3:p.Gln139=
NR_144434.1:n.628G>A
ENST00000252655.1:c.417G>A	ENSP00000252655.1:p.Gln139=
ENST00000367069.6:c.-10G>A	ENSP00000356036.1:n.-10G>A
ENST00000449822.5:c.-10G>A	ENSP00000393195.1:n.-10G>A
XM_005267153.3:c.417G>A	XP_005267210.1:p.Gln139=
XM_017011347.2:c.-258G>A	XP_016866836.1:n.-258G>A
XM_024446566.1:c.-312G>A	XP_024302334.1:n.-312G>A
XR_001743668.2:n.867G>A
XR_001743669.2:n.867G>A
XR_001743670.2:n.867G>A
XR_001743671.2:n.215G>A
XR_245553.2:n.873G>A