Canonical Allele Identifier: CA2338615031

Gene: RSPH6A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45804430G= , CM000681.2:g.45804430G=	GRCh38
NC_000019.9:g.46307688G= , CM000681.1:g.46307688G=	GRCh37
NC_000019.8:g.50999528G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221538.8:c.1475C= MANE Select	ENSP00000221538.2:p.Thr492=
ENST00000221538.7:c.1475C=	ENSP00000221538.2:p.Thr492=
ENST00000597055.1:c.1475C=	ENSP00000472630.1:p.Thr492=
ENST00000600188.5:c.683C=	ENSP00000471559.1:p.Thr228=
NM_030785.3:c.1475C=	NP_110412.1:p.Thr492=
XM_011527351.1:c.1475C=	XP_011525653.1:p.Thr492=
XM_011527351.2:c.1475C=	XP_011525653.1:p.Thr492=
NM_030785.4:c.1475C= MANE Select	NP_110412.1:p.Thr492=